Functionalized silicone polymers and methods of making and using the same

ABSTRACT

Functionalized silicone polymers incorporating segments formed from medium-chain fatty acids are generally disclosed herein. Methods of using such compounds, for example, as surfactants, are also disclosed herein, as well as methods of making such compounds, for example, from medium-chain fatty acids derived from natural oils.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. patent application Ser. No. 16/573,300, filed Sep. 17, 2019 and entitled “Functionalized Silicone Polymers and Methods of Making and Using the Same;” which claims the benefit of priority of U.S. Provisional Patent Application No. 62/732,324, filed Sep. 17, 2018 and entitled “Functionalized Silicone Polymers and Methods of Making and Using the Same;” U.S. Provisional Patent Application No. 62/732,408, filed Sep. 17, 2018 and entitled “Functionalized Silicone Polymers and Methods of Making and Using the Same;” and U.S. Provisional Patent Application No. 62/732,416, filed Sep. 17, 2018 and entitled “Functionalized Silicone Polymers and Methods of Making and Using the Same;” which are hereby incorporated by reference as though each were set forth herein in its entirety.

TECHNICAL FIELD

Functionalized silicone polymers incorporating segments from medium-chain fatty acids are generally disclosed herein. Methods of using such compounds, for example, as surfactants, are also disclosed herein, as well as methods of making such compounds, for example, from medium-chain fatty acids derived from natural oils.

BACKGROUND

Natural oils, such as seed oils, and their derivatives can provide useful starting materials for making a variety of chemical compounds. Because such compounds contain a certain degree of inherent functionality that is otherwise absent from petroleum-sourced materials, it can often be more desirable, if not cheaper, to use natural oils or their derivatives as a starting point for making certain compounds. Additionally, natural oils and their derivatives are generally sourced from renewable feedstocks. Thus, by using such starting materials, one can enjoy the concomitant advantage of developing useful chemical products without consuming limited supplies of petroleum. Further, refining natural oils can be less intensive in terms of the severity of the conditions required to carry out the refining process.

Natural oils can be refined in a variety of ways. For example, processes that rely on microorganisms can be used, such as fermentation. Chemical processes can also be used. For example, when the natural oils contain at least one carbon-carbon double bond, olefin metathesis can provide a useful means of refining a natural oil and making useful chemicals from the compounds in the feedstock.

Metathesis is a catalytic reaction that involves the interchange of alkylidene units among compounds containing one or more double bonds (e.g., olefinic compounds) via the cleavage and formation of carbon-carbon double bonds. Metathesis may occur between two like molecules (often referred to as “self-metathesis”) or it may occur between two different molecules (often referred to as “cross-metathesis”). Self-metathesis may be represented schematically as shown below in Equation (A):

R^(a)—CH═CH—R^(b)+R^(a)—CH═CH—R^(b)↔R^(a)—CH═CH—R^(a)+R^(b)—CH═CH—R^(b),  (A)

wherein R^(a) and R^(b) are organic groups.

Cross-metathesis may be represented schematically as shown below in Equation (B):

R^(a)—CH═CH—R^(b)+R^(c)—CH═CH—R^(d)↔R^(a)—CH═CH—R^(c)+R^(a)—CH═CH—R^(d)+R^(b)—CH═CH—R^(c)+R^(b)—CH═CH—R^(d),  (B)

wherein R^(a), R^(b), R^(c), and R^(d) are organic groups. Self-metathesis will also generally occur concurrently with cross-metathesis.

In recent years, there has been an increased demand for environmentally friendly techniques for manufacturing materials typically derived from petroleum sources, which can be made by processes that involve olefin metathesis. This has led to studies of the feasibility of manufacturing biofuels, waxes, plastics, and the like, using natural oil feedstocks, such as vegetable and/or seed-based oils.

Natural oil feedstocks of interest include, but are not limited to, oils such as natural oils (e.g., vegetable oils, fish oils, algae oils, and animal fats), and derivatives of natural oils, such as free fatty acids and fatty acid alkyl (e.g., methyl) esters. These natural oil feedstocks may be converted into industrially useful chemicals (e.g., waxes, plastics, cosmetics, biofuels, etc.) by any number of different metathesis reactions. Significant reaction classes include, as non-limiting examples, self-metathesis, cross-metathesis with olefins, and ring-opening metathesis reactions. Non-limiting examples of useful metathesis catalysts are described in further detail below.

Refining processes for natural oils (e.g., employing metathesis) can lead to compounds having chain lengths closer to those generally desired for chemical intermediates of specialty chemicals (e.g., about 9 to 15 carbon atoms). By using these compounds as starting materials, it is possible to create a variety of novel chemical compounds that may be used for a variety of useful purposes.

Silicone polymers are widely used in a number of contexts. The particular properties of these compounds are controlled, at least in part, by the chemical identity of the substituents on the silicon atoms in the chain of alternating silicon and oxygen atoms. In general, these substituents are hydrogen atoms, alkyl groups, such as methyl, and aryl groups, such as phenyl. This places some restrictions on the resulting properties of such silicone polymers. As a result, users are often forced to employ silicone polymers that fail to provide ideal properties, which therefore requires the addition of other ingredients to try to achieve the desired properties. Or, in some cases, it may require the use of non-silicone materials in instances where a silicone-based material would be desirable.

Further, silicone polymers are widely used. Therefore, it may be desirable to incorporate some percentage of renewably derived material into the polymers, instead of using material derived from fossil fuel sources.

Thus, there is a continuing need to develop silicone polymers that are renewably sourced, and can serve as suitable compounds for making a silicone polymers.

SUMMARY

The present disclosure provides novel silicone polymers that are derived from renewable sources and that are built from difunctional building blocks that are easy to react at the silicon atoms of the polymer.

In a first aspect, the disclosure provides siloxane polymers of formula (I):

wherein: each R¹, R², R³, and R⁴ is independently a hydrogen atom, a C₁₋₁₄ hydrocarbyl group, or a C₁₋₁₄ hydrocarbyloxy group; R^(x) and R^(y) are —(CH₂)_(n)C(═O)—R⁵; each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹); each R⁶, R⁷, R⁸, and R⁹ is independently C₁₋₂₅alkyl, C₂₋₂₅ alkenyl, or C₁₋₁₀₁ heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R^(z); R^(z) is a halogen atom, —OH, —NH₂, C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₁₂ heteroalkyl, or C₆₋₁₄ aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; each n is independently an integer ranging from 9 to 17; and k is independently an integer ranging from 5 to 5000.

In a second aspect, the disclosure provides siloxane polymers comprising a plurality of constitutional units, wherein the plurality of constitutional units comprises:

(a) constitutional units of formula (II):

and

(b) constitutional units of formula (III):

wherein: each R¹ and R² is independently a hydrogen atom, a C₃₋₁₀₁ oxyalkyl group, or a C₁₋₁₄ hydrocarbyl group, which is optionally substituted one or more times by halogen atoms; each R³ and R⁴ is independently a hydrogen atom, —(CH₂)_(n)C(═O)—R⁵, a C₃₋₁₀₁ oxyalkyl group, or a C₁₋₁₄ hydrocarbyl group, which is optionally substituted one or more times by halogen atoms, wherein, for each constitutional unit of formula (III), at least one of R³ and R⁴ is —(CH₂)_(n)C(═O)—R⁵; each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹); each R⁶, R⁷, R⁸, and R⁹ is independently C₁₋₂₅ alkyl, C₂₋₂₅ alkenyl, or C₁₋₄₀₁ heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R^(x); R^(x) is a halogen atom, —OH, —NH₂, C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₁₂ heteroalkyl, or C₆₋₁₄ aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; and each n is independently an integer ranging from 9 to 17.

In a third aspect, the disclosure provides silicone compositions, the silicone composition comprising one or more siloxane polymers of the first aspect.

In a fourth aspect, the disclosure provides articles of manufacture, which comprise a portion formed from a silicone composition of the second aspect.

Further aspects and embodiments are provided in the foregoing detailed description and claims.

DETAILED DESCRIPTION

The following description recites various aspects and embodiments of the inventions disclosed herein. No particular embodiment is intended to define the scope of the invention. Rather, the embodiments provide non-limiting examples of various compositions, and methods that are included within the scope of the claimed inventions. The description is to be read from the perspective of one of ordinary skill in the art. Therefore, information that is well known to the ordinarily skilled artisan is not necessarily included.

Definitions

The following terms and phrases have the meanings indicated below, unless otherwise provided herein. This disclosure may employ other terms and phrases not expressly defined herein. Such other terms and phrases shall have the meanings that they would possess within the context of this disclosure to those of ordinary skill in the art. In some instances, a term or phrase may be defined in the singular or plural. In such instances, it is understood that any term in the singular may include its plural counterpart and vice versa, unless expressly indicated to the contrary.

As used herein, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. For example, reference to “a substituent” encompasses a single substituent as well as two or more substituents, and the like.

As used herein, “for example,” “for instance,” “such as,” or “including” are meant to introduce examples that further clarify more general subject matter. Unless otherwise expressly indicated, such examples are provided only as an aid for understanding embodiments illustrated in the present disclosure, and are not meant to be limiting in any fashion. Nor do these phrases indicate any kind of preference for the disclosed embodiment.

As used herein, “polymer” refers to a substance having a chemical structure that includes the multiple repetition of constitutional units formed from substances of comparatively low relative molecular mass relative to the molecular mass of the polymer. The term “polymer” includes soluble and/or fusible molecules having chains of repeat units, and also includes insoluble and infusible networks. As used herein, the term “polymer” can include oligomeric compounds, which have only a few (e.g., 5-100) constitutional units.

As used herein, “silicone polymer” or “siloxane polymer” refer to a polymer that includes a series of repeating constitutional units having unsubstituted or substituted silicon atoms and oxygen atoms, e.g., —Si—O—Si—O—Si—O—Si—O—Si—O—, wherein each silicon atom is additionally attached to two hydrogen atoms, non-hydrogen substituents, or a combination thereof. In general, the silicone polymers or siloxane polymers envisioned herein have a weight-average molecular weight of at least 500 Da, or 1 kDa. Such polymers can also contain additional constitutional units, including additional non-siloxane blocks, thereby resulting in copolymers, such as graft copolymers and block copolymers. As used herein, silicone polymers or siloxane polymers includes oligomeric compounds, which have only a few (e.g., 5-100) constitutional units.

As used herein, “natural oil,” “natural feedstock,” or “natural oil feedstock” refer to oils derived from plants or animal sources. These terms include natural oil derivatives, unless otherwise indicated. The terms also include modified plant or animal sources (e.g., genetically modified plant or animal sources), unless indicated otherwise. Examples of natural oils include, but are not limited to, vegetable oils, algae oils, fish oils, animal fats, tall oils, derivatives of these oils, combinations of any of these oils, and the like. Representative non-limiting examples of vegetable oils include rapeseed oil (canola oil), coconut oil, corn oil, cottonseed oil, olive oil, palm oil, peanut oil, safflower oil, sesame oil, soybean oil, sunflower oil, linseed oil, palm kernel oil, tung oil, jatropha oil, mustard seed oil, pennycress oil, camelina oil, hempseed oil, and castor oil. Representative non-limiting examples of animal fats include lard, tallow, poultry fat, yellow grease, and fish oil. Tall oils are by-products of wood pulp manufacture. In some embodiments, the natural oil or natural oil feedstock comprises one or more unsaturated glycerides (e.g., unsaturated triglycerides). In some such embodiments, the natural oil feedstock comprises at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, or at least 95% by weight, or at least 97% by weight, or at least 99% by weight of one or more unsaturated triglycerides, based on the total weight of the natural oil feedstock.

As used herein, “natural oil derivatives” refers to the compounds or mixtures of compounds derived from a natural oil using any one or combination of methods known in the art. Such methods include but are not limited to saponification, fat splitting, transesterification, esterification, hydrogenation (partial, selective, or full), isomerization, oxidation, and reduction. Representative non-limiting examples of natural oil derivatives include gums, phospholipids, soapstock, acidulated soapstock, distillate or distillate sludge, fatty acids and fatty acid alkyl ester (e.g. non-limiting examples such as 2-ethylhexyl ester), hydroxy substituted variations thereof of the natural oil. For example, the natural oil derivative may be a fatty acid methyl ester (“FAME”) derived from the glyceride of the natural oil. In some embodiments, a feedstock includes canola or soybean oil, as a non-limiting example, refined, bleached, and deodorized soybean oil (i.e., RBD soybean oil). Soybean oil typically comprises about 95% weight or greater (e.g., 99% weight or greater) triglycerides of fatty acids. Major fatty acids in the polyol esters of soybean oil include saturated fatty acids, as a non-limiting example, palmitic acid (hexadecanoic acid) and stearic acid (octadecanoic acid), and unsaturated fatty acids, as a non-limiting example, oleic acid (9-octadecenoic acid), linoleic acid (9, 12-octadecadienoic acid), and linolenic acid (9,12,15-octadecatrienoic acid).

As used herein, “metathesis catalyst” includes any catalyst or catalyst system that catalyzes an olefin metathesis reaction.

As used herein, “metathesize” or “metathesizing” refer to the reacting of a feedstock in the presence of a metathesis catalyst to form a “metathesized product” comprising new olefinic compounds, i.e., “metathesized” compounds. Metathesizing is not limited to any particular type of olefin metathesis, and may refer to cross-metathesis (i.e., co-metathesis), self-metathesis, ring-opening metathesis, ring-opening metathesis polymerizations (“ROMP”), ring-closing metathesis (“RCM”), and acyclic diene metathesis (“ADMET”). In some embodiments, metathesizing refers to reacting two triglycerides present in a natural feedstock (self-metathesis) in the presence of a metathesis catalyst, wherein each triglyceride has an unsaturated carbon-carbon double bond, thereby forming a new mixture of olefins and esters which may include a triglyceride dimer. Such triglyceride dimers may have more than one olefinic bond, thus higher oligomers also may form. Additionally, in some other embodiments, metathesizing may refer to reacting an olefin, such as ethylene, and a triglyceride in a natural feedstock having at least one unsaturated carbon-carbon double bond, thereby forming new olefinic molecules as well as new ester molecules (cross-metathesis).

As used herein, “olefin” or “olefins” refer to compounds having at least one unsaturated carbon-carbon double bond. In certain embodiments, the term “olefins” refers to a group of unsaturated carbon-carbon double bond compounds with different carbon lengths. Unless noted otherwise, the terms “olefin” or “olefins” encompasses “polyunsaturated olefins” or “poly-olefins,” which have more than one carbon-carbon double bond. As used herein, the term “monounsaturated olefins” or “mono-olefins” refers to compounds having only one carbon-carbon double bond. A compound having a terminal carbon-carbon double bond can be referred to as a “terminal olefin,” while an olefin having a non-terminal carbon-carbon double bond can be referred to as an “internal olefin.”

As used herein, the term “low-molecular-weight olefin” may refer to any one or combination of unsaturated straight, branched, or cyclic hydrocarbons in the C₂₋₁₄ range. Low-molecular-weight olefins include “alpha-olefins” or “terminal olefins,” wherein the unsaturated carbon-carbon bond is present at one end of the compound. Low-molecular-weight olefins may also include dienes or trienes. Low-molecular-weight olefins may also include internal olefins or “low-molecular-weight internal olefins.” In certain embodiments, the low-molecular-weight internal olefin is in the C₄₋₁₄ range. Examples of low-molecular-weight olefins in the C₂₋₆ range include, but are not limited to: ethylene, propylene, 1-butene, 2-butene, isobutene, 1-pentene, 2-pentene, 3-pentene, 2-methyl-1-butene, 2-methyl-2-butene, 3-methyl-1-butene, cyclopentene, 1,4-pentadiene, 1-hexene, 2-hexene, 3-hexene, 4-hexene, 2-methyl-1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 2-methyl-2-pentene, 3-methyl-2-pentene, 4-methyl-2-pentene, 2-methyl-3-pentene, and cyclohexene. Non-limiting examples of low-molecular-weight olefins in the C₇₋₉ range include 1,4-heptadiene, 1-heptene, 3,6-nonadiene, 3-nonene, 1,4,7-octatriene. Other possible low-molecular-weight olefins include styrene and vinyl cyclohexane. In certain embodiments, it is preferable to use a mixture of olefins, the mixture comprising linear and branched low-molecular-weight olefins in the C₄₋₁₀ range. In one embodiment, it may be preferable to use a mixture of linear and branched C₄ olefins (i.e., combinations of: 1-butene, 2-butene, and/or isobutene). In other embodiments, a higher range of C₁₁₋₁₄ may be used.

In some instances, the olefin can be an “alkene,” which refers to a straight- or branched-chain non-aromatic hydrocarbon having 2 to 30 carbon atoms and one or more carbon-carbon double bonds, which may be optionally substituted, as herein further described, with multiple degrees of substitution being allowed. A “monounsaturated alkene” refers to an alkene having one carbon-carbon double bond, while a “polyunsaturated alkene” refers to an alkene having two or more carbon-carbon double bonds. A “lower alkene,” as used herein, refers to an alkene having from 2 to 10 carbon atoms.

As used herein, “alpha-olefin” refers to an olefin (as defined above) that has a terminal carbon-carbon double bond. In some embodiments, the alpha-olefin is a terminal alkene, which is an alkene (as defined above) having a terminal carbon-carbon double bond. Additional carbon-carbon double bonds can be present.

As used herein, “ester” or “esters” refer to compounds having the general formula: R—COO—R′, wherein R and R′ denote any organic group (such as alkyl, aryl, or silyl groups) including those bearing heteroatom-containing substituent groups. In certain embodiments, R and R′ denote alkyl, alkenyl, aryl, or alcohol groups. In certain embodiments, the term “esters” may refer to a group of compounds with the general formula described above, wherein the compounds have different carbon lengths. In certain embodiments, the esters may be esters of glycerol, which is a trihydric alcohol. The term “glyceride” can refer to esters where one, two, or three of the —OH groups of the glycerol have been esterified.

It is noted that an olefin may also comprise an ester, and an ester may also comprise an olefin, if the R or R′ group in the general formula R—COO—R′ contains an unsaturated carbon-carbon double bond. Such compounds can be referred to as “unsaturated esters” or “olefin esters.” Further, a “terminal olefin ester” may refer to an ester compound where R has an olefin positioned at the end of the chain. An “internal olefin ester” may refer to an ester compound where R has an olefin positioned at an internal location on the chain. Additionally, the term “terminal olefin” may refer to an ester or an acid thereof where R′ denotes hydrogen or any organic compound (such as an alkyl, aryl, or silyl group) and R has an olefin positioned at the end of the chain, and the term “internal olefin” may refer to an ester or an acid thereof where R′ denotes hydrogen or any organic compound (such as an alkyl, aryl, or silyl group) and R has an olefin positioned at an internal location on the chain.

As used herein, “hydrocarbon” refers to an organic group composed of carbon and hydrogen, which can be saturated or unsaturated, and can include aromatic groups. The term “hydrocarbyl” refers to a monovalent or polyvalent hydrocarbon moiety.

As used herein, “alkyl” refers to a straight or branched chain saturated hydrocarbon having 1 to 30 carbon atoms, which may be optionally substituted, as herein further described, with multiple degrees of substitution being allowed. Examples of “alkyl,” as used herein, include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, isobutyl, n-butyl, sec-butyl, tert-butyl, isopentyl, n-pentyl, neopentyl, n-hexyl, and 2-ethylhexyl. The number of carbon atoms in an alkyl group is represented by the phrase “C_(x-y) alkyl,” which refers to an alkyl group, as herein defined, containing from x to y, inclusive, carbon atoms. Thus, “C₁₋₆ alkyl” represents an alkyl chain having from 1 to 6 carbon atoms and, for example, includes, but is not limited to, methyl, ethyl, n-propyl, isopropyl, isobutyl, n-butyl, sec-butyl, tert-butyl, isopentyl, n-pentyl, neopentyl, and n-hexyl. In some instances, the “alkyl” group can be divalent, in which case the group can alternatively be referred to as an “alkylene” group. Also, in some instances, one or more of the carbon atoms in the alkyl or alkylene group can be replaced by a heteroatom (e.g., selected from nitrogen, oxygen, or sulfur, including quaternary nitrogen atoms, N-oxides, sulfur oxides, and sulfur dioxides, where feasible), and is referred to as a “heteroalkyl” or “heteroalkylene” group, respectively. Non-limiting examples include “oxyalkyl” or “oxyalkylene” groups, which are groups of the following formulas: -[-(alkylene)-O-]_(v)-alkyl, or -[-(alkylene)-O-]_(v)-alkylene-, respectively, where v is 1 or more, such as 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or the like.

As used herein, “alkenyl” refers to a straight or branched chain non-aromatic hydrocarbon having 2 to 30 carbon atoms and having one or more carbon-carbon double bonds, which may be optionally substituted, as herein further described, with multiple degrees of substitution being allowed. Examples of “alkenyl,” as used herein, include, but are not limited to, ethenyl, 2-propenyl, 2-butenyl, and 3-butenyl. The number of carbon atoms in an alkenyl group is represented by the phrase “C_(x-y) alkenyl,” which refers to an alkenyl group, as herein defined, containing from x to y, inclusive, carbon atoms. Thus, “C₂₋₆ alkenyl” represents an alkenyl chain having from 2 to 6 carbon atoms and, for example, includes, but is not limited to, ethenyl, 2-propenyl, 2-butenyl, and 3-butenyl. In some instances, the “alkenyl” group can be divalent, in which case the group can alternatively be referred to as an “alkenylene” group.

As used herein, “halogen” or “halo” refers to a fluorine, chlorine, bromine, and/or iodine atom. In some embodiments, the terms refer to fluorine or chlorine. As used herein, “haloalkyl” or “haloalkoxy” refer to alkyl or alkoxy groups, respectively, substituted by one or more halogen atoms. The terms “perfluoroalkyl” or “perfluoroalkoxy” refer to alkyl groups and alkoxy groups, respectively, where every available hydrogen is replaced by fluorine.

As used herein, “aryl” refers to a 6- to 30-membered cyclic, aromatic hydrocarbon, which may be optionally substituted as herein further described, with multiple degrees of substitution being allowed. Examples of “aryl” groups as used herein include, but are not limited to, phenyl and naphthyl. As used herein, the term “aryl” also includes ring systems in which a phenyl or naphthyl group is optionally fused with one to three non-aromatic, saturated or unsaturated, carbocyclic rings. For example, “aryl” would include ring systems such as indene, with attachment possible to either the aromatic or the non-aromatic ring(s).

As used herein, “substituted” refers to substitution of one or more hydrogen atoms of the designated moiety with the named substituent or substituents, multiple degrees of substitution being allowed unless otherwise stated, provided that the substitution results in a stable or chemically feasible compound. A stable compound or chemically feasible compound is one in which the chemical structure is not substantially altered when kept at a temperature from about −80° C. to about +40° C., in the absence of moisture or other chemically reactive conditions, for at least a week. As used herein, the phrases “substituted with one or more . . . ” or “substituted one or more times . . . ” refer to a number of substituents that equals from one to the maximum number of substituents possible based on the number of available bonding sites, provided that the above conditions of stability and chemical feasibility are met.

As used herein, “mix” or “mixed” or “mixture” refers broadly to any combining of two or more compositions. The two or more compositions need not have the same physical state; thus, solids can be “mixed” with liquids, e.g., to form a slurry, suspension, or solution. Further, these terms do not require any degree of homogeneity or uniformity of composition. This, such “mixtures” can be homogeneous or heterogeneous, or can be uniform or non-uniform. Further, the terms do not require the use of any particular equipment to carry out the mixing, such as an industrial mixer.

As used herein, “optionally” means that the subsequently described event(s) may or may not occur. In some embodiments, the optional event does not occur. In some other embodiments, the optional event does occur one or more times.

As used herein, “comprise” or “comprises” or “comprising” or “comprised of” refer to groups that are open, meaning that the group can include additional members in addition to those expressly recited. For example, the phrase, “comprises A” means that A must be present, but that other members can be present too. The terms “include,” “have,” and “composed of” and their grammatical variants have the same meaning. In contrast, “consist of” or “consists of” or “consisting of” refer to groups that are closed. For example, the phrase “consists of A” means that A and only A is present.

As used herein, “or” is to be given its broadest reasonable interpretation, and is not to be limited to an either/or construction. Thus, the phrase “comprising A or B” means that A can be present and not B, or that B is present and not A, or that A and B are both present. Further, if A, for example, defines a class that can have multiple members, e.g., A₁ and A₂, then one or more members of the class can be present concurrently.

As used herein, the various functional groups represented will be understood to have a point of attachment at the functional group having the hyphen or dash (—) or an asterisk (*). In other words, in the case of —CH₂CH₂CH₃, it will be understood that the point of attachment is the CH₂ group at the far left. If a group is recited without an asterisk or a dash, then the attachment point is indicated by the plain and ordinary meaning of the recited group.

In some instances herein, organic compounds are described using the “line structure” methodology, where chemical bonds are indicated by a line, where the carbon atoms are not expressly labeled, and where the hydrogen atoms covalently bound to carbon (or the C—H bonds) are not shown at all. For example, by that convention, the formula

represents n-propane. In some instances herein, a squiggly bond is used to show the compound can have any one of two or more isomers. For example, the structure

can refer to (E)-2-butene or (Z)-2-butene.

As used herein, multi-atom bivalent species are to be read from left to right. For example, if the specification or claims recite A-D-E and D is defined as —OC(O)—, the resulting group with D replaced is: A-OC(O)-E and not A-C(O)O-E.

Other terms are defined in other portions of this description, even though not included in this subsection.

Siloxane Polymers

In a one or more aspects, the disclosure provides siloxane polymers of formula (I):

wherein: each R¹, R², R³, and R⁴ is independently a hydrogen atom, a C₁₋₁₄ hydrocarbyl group, or a C₁₋₁₄ hydrocarbyloxy group; R^(x) and R^(y) are —(CH₂)_(n)C(═O)—R⁵; each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹); each R⁶, R⁷, R⁸, and R⁹ is independently C₁₋₂₅alkyl, C₂₋₂₅ alkenyl, or C₁₋₁₀₁ heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R^(z); R^(z) is a halogen atom, —OH, —NH₂, C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₁₂ heteroalkyl, or C₆₋₁₄ aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; each n is independently an integer ranging from 9 to 17; and k is independently an integer ranging from 5 to 5000.

As noted above, the siloxane polymers disclosed herein contain one or more moieties of the formula —(CH₂)_(n)C(═O)—R⁵. Such moieties can be derived from any suitable source. In some embodiments, such moieties are derived from renewable sources, such as seed oils. For example, metathesis chemistry can be employed to transform unsaturated fatty acids of seed oils to terminally unsaturated fatty acids (or esters thereof), such as 9-decenoic acid, 10-undecenoic acid, or 11-dodecenoic acid (or esters thereof). Such acids or esters can, in some embodiments, be further functionalized according to the various groups that make up the scope of R⁵.

The integer n can have any suitable value, and may depend on the intermediate from which the substituent is derived. For example, in some instances, such substituents can be derived from esters having a terminal olefin group, which reacts with a siloxyl group to replace the Si—O bond with a Si—C bond of the substituent. In some embodiments, the substituent is derived from esters of 9-decenoic acid, such that the value of n is 9. In some other embodiments, the substituent is derived from esters of 10-undecenoic acid, such that the value of n is 10. In some other embodiments, the substituent is derived from esters of 11-dodecenoic acid, such that the value of n is 11. The same applies for higher-order homologs. Thus, in some embodiments, n is an integer ranging from 9 to 17, or from 10 to 17, or from 11 to 17, or from 11 to 15, or from 11 to 14. In some such embodiments, n is 9, or n is 10, or n is 11, or n is 12, or n is 13, or n is 14, or n is 15, or n is 16, or n is 17. In some embodiments, n is 9, 10, or 11. In some such embodiments, n is 9 or 11.

The moiety R⁵ can have any suitable value. In some embodiments, each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹). As used this context and in other similar contexts in the present disclosure, the term “independently” or “independent” refers to the fact that the constitutional unit may occur in the polymer a plurality of times, and that the value of a particular variable, such as R⁵, for one such occurrence is independent of its value for another occurrence. In general, throughout the present disclosure, the real-atom value of any variable for a particular occurrence of a constitutional unit is independent of the real-atom value of that variable for another occurrence of the constitutional unit, unless it is so stated, for example, by stating something akin to “each R⁵ is —OCH₃,” or like phrasing with respect to a real-atom group.

In some such embodiments, each R⁵ is independently —O—R⁶. The variable R⁶ can have any suitable value. In some embodiments, each R⁶ is independently C₁₋₁₂alkyl. In some such embodiments, each R⁶ is independently methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, or 2-ethylhexyl. In some further such embodiments, each R⁶ is independently methyl, ethyl, or isopropyl. In some even further such embodiments, each R⁶ is independently methyl or ethyl. In some even further such embodiments each R⁶ is methyl.

In some other embodiments, each R⁶ is independently C₃401 oxyalkyl. In some such embodiments, each R⁶ is independently —(CH₂—CH₂—O)_(w)—CH₃, wherein w is an integer ranging from 1 to 200, or from 1 to 100, or from 1 to 50, or from 1 to 25. In some further such embodiments, each w is independently an integer ranging from 1 to 40, or from 1 to 30, or from 1 to 20, such as 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20.

In some other embodiments, each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more —OH groups, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group. In some such embodiments, each R⁶ is independently —(CH₂)_(x)—CH(O)CH₂, wherein x is an integer ranging from 1 to 12. In some further such embodiments, each x is independently an integer ranging from 1 to 6, such as 1, 2, 3, 4, 5, or 6. In some even further such embodiments, each x is 1.

In some other embodiments, each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more halogen atoms, such as fluorine atoms or chlorine atoms. In some such embodiments, each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more fluorine atoms. In some even further such embodiments, each R⁶ is independently —(CH₂)_(y)—(CF₂)_(z)—CF₃, wherein each y and each z is independently an integer ranging from 0 to 12, or from 0 to 6, or from 0 to 3. In some even further such embodiments, each y is independently 1, 2, or 3, and each z is independently 1, 2, 3, or 4.

In some instances, R⁵ can have other values. For example, in some embodiments, each R⁵ is independently —NH—R⁷. In some such embodiments, each R⁷ is independently a moiety of formula (IV):

-G³-N⁺—(R¹¹)(R¹²)-G⁴-R¹³  (IV)

wherein: each G³ is independently C₁₋₁₂alkylene; each G⁴ is independently C₁₋₆alkylene; each R¹¹ and each R¹² are independently a hydrogen atom or C₁₋₂₀ alkyl; and each R¹³ is independently a hydrogen atom or a phenyl moiety. In some further such embodiments, each G³ is independently —(CH₂)_(p)—, wherein each p is independently an integer ranging from 1 to 6, such as 1, 2, 3, 4, 5, or 6. In some even further such embodiments, each G⁴ is independently —(CH₂)_(q)—, wherein each q is independently an integer ranging from 1 to 3, such as 1, 2, or 3. In some even further such embodiments, each R¹¹ and each R¹² are independently C₁₋₆alkyl. In some even further embodiments, each R¹¹ and each R¹² are independently methyl, ethyl, or isopropyl. In some even further embodiments, each R¹¹ and each R¹² are independently methyl or ethyl. In some even further embodiments, each R¹¹ and each R¹² is methyl. In some further embodiments of any of the foregoing embodiments, each R¹³ is a phenyl moiety.

In some such embodiments, each R⁵ is independently —N(R⁸)(R⁹). The variables R⁸ and R⁹ can have any suitable value. In some embodiments, each R⁷ and R⁸ is independently C₁₋₁₂ alkyl. In some such embodiments, each R⁸ and R⁹ is independently methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, or 2-ethylhexyl. In some further such embodiments, each R⁸ and R⁹ is independently methyl, ethyl, or isopropyl. In some even further such embodiments, each R⁸ and R⁹ is independently methyl or ethyl. In some even further such embodiments each R⁸ and R⁹ is methyl.

In some embodiments, each R¹, R², R³, and R⁴ is independently a hydrogen atom, a C₁₋₁₄ hydrocarbyl group, or a C₁₋₁₄ hydrocarbyloxy group. In some such embodiments, each R¹, R², R³, and R⁴ is independently a C₁₋₁₄ hydrocarbyl group. In some further such embodiments, each R¹, R², R³, and R⁴ is independently a C₁₋₈ alkyl group. In some even further embodiments, each R¹, R², R³, and R⁴ is independently selected from the group consisting of methyl, ethyl, propyl, and isopropyl. In some even further embodiments, each R¹, R², R³, and R⁴ is independently selected from the group consisting of methyl and ethyl. In some even further embodiments, each R¹, R², R³, and R⁴ is methyl.

In some embodiments, most, but not all, of R¹, R², R³, and R⁴ are independently C₁₋₆alkyl (such as methyl, ethyl, or isopropyl). In some such embodiments, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, of all R¹, R², R³, and R⁴ in each segment of formula (I) are independently C₁₋₆alkyl (such as methyl, ethyl, or isopropyl), and the remaining R¹, R², R³, and R⁴ are independently a hydrogen atom or C₁₋₆alkoxy (such as methoxy, ethoxy, or isopropoxy). In some further such embodiments, at least one of R¹, R², R³, and R⁴ in each segment of formula (I) in the polymer is a hydrogen atom. In some further such embodiments, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, of all R¹, R², R³, and R⁴ in each segment of formula (I) are independently C₁₋₆alkyl (such as methyl, ethyl, or isopropyl), and the remaining R¹, R², R³, and R⁴ are independently a C₁₋₆alkoxy (such as methoxy, ethoxy, or isopropoxy).

The siloxane polymers of any of the above embodiments can have any suitable physical properties. For example, in some embodiments, the siloxane polymer has a molecular weight ranging from 1 kDa to 50 kDa.

In a certain other aspects, the disclosure provides siloxane polymers comprising a plurality of constitutional units, wherein the plurality of constitutional units comprises:

(a) constitutional units of formula (II):

and

(b) constitutional units of formula (III):

wherein: each R¹ and R² is independently a hydrogen atom, a C₃₋₁₀₁ oxyalkyl group, or a C₁₋₁₄ hydrocarbyl group, which is optionally substituted one or more times by halogen atoms; each R³ and R⁴ is independently a hydrogen atom, —(CH₂)_(n)C(═O)—R⁵, a C₃₋₁₀₁ oxyalkyl group, or a C₁₋₁₄ hydrocarbyl group, which is optionally substituted one or more times by halogen atoms, wherein, for each constitutional unit of formula (III), at least one of R³ and R⁴ is —(CH₂)_(n)C(═O)—R⁵; each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹); each R⁶, R⁷, R⁸, and R⁹ is independently C₁₋₂₅ alkyl, C₂₋₂₅ alkenyl, or C₁₋₄₀₁ heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R^(x); R^(x) is a halogen atom, —OH, —NH₂, C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₁₂ heteroalkyl, or C₆₋₁₄ aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; and each n is independently an integer ranging from 9 to 17.

As noted above, the siloxane polymers disclosed herein contain one or more moieties of the formula —(CH₂)_(n)C(═O)—R⁵. Such moieties can be derived from any suitable source. In some embodiments, such moieties are derived from renewable sources, such as seed oils. For example, metathesis chemistry can be employed to transform unsaturated fatty acids of seed oils to terminally unsaturated fatty acids (or esters thereof), such as 9-decenoic acid, 10-undecenoic acid, or 11-dodecenoic acid (or esters thereof). Such acids or esters can, in some embodiments, be further functionalized according to the various groups that make up the scope of R⁵.

The integer n can have any suitable value, and may depend on the intermediate from which the substituent is derived. For example, in some instances, such substituents can be derived from esters having a terminal olefin group, which reacts with a siloxyl group to replace the Si—O bond with a Si—C bond of the substituent. In some embodiments, the substituent is derived from esters of 9-decenoic acid, such that the value of n is 9. In some other embodiments, the substituent is derived from esters of 10-undecenoic acid, such that the value of n is 10. In some other embodiments, the substituent is derived from esters of 11-dodecenoic acid, such that the value of n is 11. The same applies for higher-order homologs. Thus, in some embodiments, n is an integer ranging from 9 to 17, or from 10 to 17, or from 11 to 17, or from 11 to 15, or from 11 to 14. In some such embodiments, n is 9, or n is 10, or n is 11, or n is 12, or n is 13, or n is 14, or n is 15, or n is 16, or n is 17. In some embodiments, n is 9, 10, or 11. In some such embodiments, n is 9 or 11. In some embodiments, the siloxane polymer includes moieties according to the formula —(CH₂)_(n)C(═O)—R⁵, where n is 9 for some such moieties and n is 11 for other such moieties. In such embodiments, the numerical ratio of substituents having n is 9 to those having n is 11 ranges from 1:10 to 10:1, or 1:5 to 5:1, or from 1:3 to 3:1, or from 1:2 to 2:1. In some cases, substituents where n is 9 may be present in amounts at least the same as substituents where n is 11. For example, in some such embodiments, the numerical ratio of substituents having n is 9 to those having n is 11 ranges from 1:1 to 10:1, or 1:1 to 5:1, or from 1:1 to 3:1, or from 1:1 to 2:1.

The moiety R⁵ can have any suitable value. In some embodiments, each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹). As used this context and in other similar contexts in the present disclosure, the term “independently” or “independent” refers to the fact that the constitutional unit may occur in the polymer a plurality of times, and that the value of a particular variable, such as R⁵, for one such occurrence is independent of its value for another occurrence. In general, throughout the present disclosure, the real-atom value of any variable for a particular occurrence of a constitutional unit is independent of the real-atom value of that variable for another occurrence of the constitutional unit, unless it is so stated, for example, by stating something akin to “each R⁵ is —OCH₃,” or like phrasing with respect to a real-atom group.

In some such embodiments, each R⁵ is independently —O—R⁶. The variable R⁶ can have any suitable value. In some embodiments, each R⁶ is independently C₁₋₁₂alkyl. In some such embodiments, each R⁶ is independently methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, or 2-ethylhexyl. In some further such embodiments, each R⁶ is independently methyl, ethyl, or isopropyl. In some even further such embodiments, each R⁶ is independently methyl or ethyl. In some even further such embodiments each R⁶ is methyl.

In some other embodiments, each R⁶ is independently C₃₋₄₀₁ oxyalkyl. In some such embodiments, each R⁶ is independently —(CH₂—CH₂—O)_(w)—CH₃, wherein w is an integer ranging from 1 to 200, or from 1 to 100, or from 1 to 50, or from 1 to 25. In some further such embodiments, each w is independently an integer ranging from 1 to 40, or from 1 to 30, or from 1 to 20, such as 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20.

In some other embodiments, each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more —OH groups, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group. In some such embodiments, each R⁶ is independently —(CH₂)_(x)—CH(O)CH₂, wherein x is an integer ranging from 1 to 12. In some further such embodiments, each x is independently an integer ranging from 1 to 6, such as 1, 2, 3, 4, 5, or 6. In some even further such embodiments, each x is 1.

In some other embodiments, each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more halogen atoms, such as fluorine atoms or chlorine atoms. In some such embodiments, each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more fluorine atoms. In some even further such embodiments, each R⁶ is independently —(CH₂)_(y)—(CF₂)_(z)—CF₃, wherein each y and each z is independently an integer ranging from 0 to 12, or from 0 to 6, or from 0 to 3. In some even further such embodiments, each y is independently 1, 2, or 3, and each z is independently 1, 2, 3, or 4.

In some instances, R⁵ can have other values. For example, in some embodiments, each R⁵ is independently —NH—R⁷. In some such embodiments, each R⁷ is independently a moiety of formula (IV):

-G³-N⁺—(R¹¹)(R¹²)-G⁴-R¹³  (IV)

wherein: each G³ is independently C₁₋₁₂alkylene; each G⁴ is independently C₁₋₆alkylene; each R¹¹ and each R¹² are independently a hydrogen atom or C₁₋₂₀ alkyl; and each R¹³ is independently a hydrogen atom or a phenyl moiety. In some further such embodiments, each G³ is independently —(CH₂)_(p)—, wherein each p is independently an integer ranging from 1 to 6, such as 1, 2, 3, 4, 5, or 6. In some even further such embodiments, each G⁴ is independently —(CH₂)_(q)—, wherein each q is independently an integer ranging from 1 to 3, such as 1, 2, or 3. In some even further such embodiments, each R¹¹ and each R¹² are independently C₁₋₆alkyl. In some even further embodiments, each R¹¹ and each R¹² are independently methyl, ethyl, or isopropyl. In some even further embodiments, each R¹¹ and each R¹² are independently methyl or ethyl. In some even further embodiments, each R¹¹ and each R¹² is methyl. In some further embodiments of any of the foregoing embodiments, each R¹³ is a phenyl moiety.

In some such embodiments, each R⁵ is independently —N(R⁸)(R⁹). The variables R⁸ and R⁹ can have any suitable value. In some embodiments, each R⁸ and R⁹ is independently C₁₋₁₂ alkyl. In some such embodiments, each R⁸ and R⁹ is independently methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, or 2-ethylhexyl. In some further such embodiments, each R⁸ and R⁹ is independently methyl, ethyl, or isopropyl. In some even further such embodiments, each R⁸ and R⁹ is independently methyl or ethyl. In some even further such embodiments each R⁸ and R⁹ is methyl.

The siloxane polymers disclosed herein can contain additional constitutional units besides those of formula (II) and formula (III). For example, the siloxane polymers can be copolymers, which have additional constitutional units interspersed with those of formula (II) and formula (III). In some other cases, the siloxane polymers can be block copolymers or graft copolymers, where the polymer contains, for example, other non-siloxane segments or blocks. Thus, in some embodiments, in the siloxane polymers disclosed herein, the constitutional units of formula (II) and the constitutional units of formula (III) together make up at least 10% by weight, or at least 20% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, of the constitutional units in the siloxane polymer. In some further embodiments of the foregoing embodiments, in the siloxane polymers disclosed herein, the constitutional units of formula (II) and the constitutional units of formula (III) together make up no more than 60% by weight, or no more than 70% by weight, or no more than 80% by weight, or no more than 90% by weight, or no more than 95% by weight, or no more than 97% by weight, or no more than 99% by weight, of the constitutional units in the siloxane polymer.

The siloxane polymers disclosed herein can contain any suitable amount of the constitutional units of formula (II). Thus, in some embodiments, in the siloxane polymers disclosed herein, the constitutional units of formula (II) make up at least 1% by weight, or at least 3% by weight, or at least 5% by weight, or at least 10% by weight, or at least 20% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, of the constitutional units in the siloxane polymer. In some further embodiments of any of the foregoing embodiments, in the siloxane polymers disclosed herein, the constitutional units of formula (II) make up no more than 10% by weight, or no more than 20% by weight, or no more than 30% by weight, or no more than 40% by weight, or no more than 50% by weight, or no more than 60% by weight, or no more than 70% by weight, or no more than 80% by weight, of the constitutional units in the siloxane polymer.

The siloxane polymers disclosed herein can contain any suitable amount of the constitutional units of formula (III). Thus, in some embodiments, in the siloxane polymers disclosed herein, the constitutional units of formula (III) make up at least 1% by weight, or at least 3% by weight, or at least 5% by weight, or at least 10% by weight, or at least 20% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, of the constitutional units in the siloxane polymer. In some further embodiments of any of the foregoing embodiments, in the siloxane polymers disclosed herein, the constitutional units of formula (III) make up no more than 10% by weight, or no more than 20% by weight, or no more than 30% by weight, or no more than 40% by weight, or no more than 50% by weight, or no more than 60% by weight, or no more than 70% by weight, or no more than 80% by weight, of the constitutional units in the siloxane polymer.

The constitutional units of formula (II) and the constitutional units of formula (III) can be present in the siloxane polymer in any suitable relative amounts. For example, in the siloxane polymers disclosed herein, the numerical ratio of constitutional units of formula (II) to constitutional units of formula (III) in the siloxane polymer ranges from 1:10 to 10:1, or from 1:7 to 7:1, or from 1:5 to 5:1, or from 1:4 to 4:1, or from 1:3 to 3:1, or from 1:2 to 2:1. In some other embodiments, the numerical ratio of constitutional units of formula (II) to constitutional units of formula (III) in the siloxane polymer ranges from 1:1 to 10:1, or from 1:1 to 7:1, or from 1:1 to 5:1, or from 1:1 to 4:1, or from 1:1 to 3:1, or from 1:1 to 2:1. In some other embodiments, the numerical ratio of constitutional units of formula (III) to constitutional units of formula (II) in the siloxane polymer ranges from 1:1 to 10:1, or from 1:1 to 7:1, or from 1:1 to 5:1, or from 1:1 to 4:1, or from 1:1 to 3:1, or from 1:1 to 2:1.

As noted above, each constitutional unit of formula (II) in the siloxane polymer can have different values for R¹ and R² with each occurrence. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a hydrogen atom. Even so, in some embodiments, of the constitutional units of formula (II) in the siloxane polymer, no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a hydrogen atom, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some embodiments, of the constitutional units of formula (II) in the siloxane polymer, none of R¹ and R² is a hydrogen atom.

In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₃₋₁₀₁ oxyalkyl group. Even so, In some embodiments, of the constitutional units of formula (II) in the siloxane polymer, no more than 60% by number, or no more than 50% by number, or no more than 40% by number, or no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a C₃₋₁₀₁ oxyalkyl group, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some embodiments, of the constitutional units of formula (II) in the siloxane polymer, none of R¹ and R² is a C₃₋₁₀₁ oxyalkyl group.

In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, no more than 60% by number, or no more than 50% by number, or no more than 40% by number, or no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some embodiments, of the constitutional units of formula (II) in the siloxane polymer, none of R¹ and R² is a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms.

In embodiments where at least one occurrence of R¹ or R² is a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms, the fluoro-substituted hydrocarbyl group can be any suitable such groups. For example, in some embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₁₋₆alkyl group substituted one or more times by fluorine atoms. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, no more than 60% by number, or no more than 50% by number, or no more than 40% by number, or no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a C₁₋₆alkyl group substituted one or more times by fluorine atoms, based on twice the total number of constitutional units of formula (II) in the siloxane polymer.

In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is an unsubstituted C₁₋₁₄ hydrocarbyl group. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are an unsubstituted C₁₋₁₄ hydrocarbyl group, based on twice the total number of constitutional units of formula (I) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (I) in the siloxane polymer, all of R¹ and R² are an unsubstituted C₁₋₁₄ hydrocarbyl group.

In some further such embodiments, wherein at least one occurrence of R¹ or R² is an unsubstituted C₁₋₁₄ hydrocarbyl group, the hydrocarbyl group can be any suitable group. For example, in some embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₁₋₆alkyl group. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are a C₁₋₆alkyl group, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, all of R¹ and R² are a C₁₋₆alkyl group.

In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a substituent selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, all of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl.

In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a substituent selected from the group consisting of methyl, ethyl, and isopropyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, and isopropyl, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, all of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, and isopropyl.

In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is a substituent selected from the group consisting of methyl and ethyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are substituents selected from the group consisting of methyl and ethyl, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, all of R¹ and R² are substituents selected from the group consisting of methyl and ethyl.

In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least one occurrence of R¹ or R² is methyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² methyl, based on twice the total number of constitutional units of formula (II) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, all of R¹ and R² are methyl.

As noted above, each constitutional unit of formula (III) in the siloxane polymer can have different values for R¹ and R² with each occurrence. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a hydrogen atom. Even so, in some embodiments, of the constitutional units of formula (III) in the siloxane polymer, no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a hydrogen atom, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some embodiments, of the constitutional units of formula (III) in the siloxane polymer, none of R¹ and R² is a hydrogen atom.

In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₃₋₁₀₁ oxyalkyl group. Even so, In some embodiments, of the constitutional units of formula (III) in the siloxane polymer, no more than 60% by number, or no more than 50% by number, or no more than 40% by number, or no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a C₃₋₁₀₁ oxyalkyl group, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some embodiments, of the constitutional units of formula (III) in the siloxane polymer, none of R¹ and R² is a C₃₋₁₀₁ oxyalkyl group.

In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, no more than 60% by number, or no more than 50% by number, or no more than 40% by number, or no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some embodiments, of the constitutional units of formula (III) in the siloxane polymer, none of R¹ and R² is a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms.

In embodiments where at least one occurrence of R¹ or R² is a C₁₋₁₄ hydrocarbyl group substituted one or more times by fluorine atoms, the fluoro-substituted hydrocarbyl group can be any suitable such groups. For example, in some embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₁₋₆alkyl group substituted one or more times by fluorine atoms. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, no more than 60% by number, or no more than 50% by number, or no more than 40% by number, or no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, or no more than 3% by number, or no more than 1% by number, of R¹ and R² are a C₁₋₆alkyl group substituted one or more times by fluorine atoms, based on twice the total number of constitutional units of formula (III) in the siloxane polymer.

In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is an unsubstituted C₁₋₁₄ hydrocarbyl group. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are an unsubstituted C₁₋₁₄ hydrocarbyl group, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, all of R¹ and R² are an unsubstituted C₁₋₁₄ hydrocarbyl group.

In some further such embodiments, wherein at least one occurrence of R¹ or R² is an unsubstituted C₁₋₁₄ hydrocarbyl group, the hydrocarbyl group can be any suitable group. For example, in some embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a C₁₋₆alkyl group. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are a C₁₋₆alkyl group, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, all of R¹ and R² are a C₁₋₆alkyl group.

In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a substituent selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, all of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl.

In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a substituent selected from the group consisting of methyl, ethyl, and isopropyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, and isopropyl, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, all of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, and isopropyl.

In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is a substituent selected from the group consisting of methyl and ethyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² are substituents selected from the group consisting of methyl and ethyl, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, all of R¹ and R² are substituents selected from the group consisting of methyl and ethyl.

In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least one occurrence of R¹ or R² is methyl. In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, or at least 97% by number, or at least 99% by number, of R¹ and R² methyl, based on twice the total number of constitutional units of formula (III) in the siloxane polymer. In some further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, all of R¹ and R² are methyl.

As noted above, on each occurrence of a constitutional unit of formula (III), at least one of R¹ or R² (or both) is a moiety of the formula —(CH₂)_(n)C(═O)—R⁵ (according to any of the embodiments set forth above for this moiety). In some embodiments of any of the foregoing embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 50% by number, or at least 55% by number, or at least 60% by number, or at least 65% by number, or at least 70% by number, or at least 75% by number, of R¹ and R² are —(CH₂)_(n)C(═O)—R⁵ (according to any of the embodiments set forth above for this moiety), based on twice the total number of constitutional units of formula (III) in the siloxane polymer.

In general, the siloxane polymers disclosed herein contain two or more endcap groups. The endcap groups can have any suitable chemical structure, but are generally silane- or siloxane-based moieties. In some embodiments, the endcap groups are moieties of formula (V):

—(O)_(m)—Si(R²¹)(R²²)(R²³)  (V)

wherein: R²¹, R²², and R²³ are independently a hydrogen atom, —OH, C₁₋₁₄ hydrocarbyl, or C₁₋₁₄ hydrocarbyloxy; and m is 0 or 1. In general, the value of m will vary on the chemical functionality of the group that the group is capping. For example, if the endcap group is capping a moiety that otherwise terminates in an oxygen atom, then m is typically 0, as the siloxane polymers disclosed herein do not generally contain peroxide functionality in the backbone of the polymer. On the other hand, in embodiments where the endcap group is capping a moiety that otherwise terminates in silicon or carbon, then m is 1.

In some such embodiments, at least two of R²¹, R²², and R²³ is a hydrogen atom or C₁₋₁₄ hydrocarbyl. In some further such embodiments, at least two of R²¹, R²², and R²³ is C₁₋₁₄ hydrocarbyl. In some even further such embodiments, at least two of R²¹, R²², and R²³ are selected independently from the group consisting of: methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, or neopentyl. In some even further such embodiments, at least two of R²¹, R²², and R²³ are methyl.

In some further embodiments of any of the aforementioned embodiments, one of R²¹, R²², and R²³ is a —OH or C₁₋₁₄ hydrocarbyloxy. In some further such embodiments, one of R²¹, R²², and R²³ is C₁₋₁₄ hydrocarbyloxy. In some even further such embodiments, one of R²¹, R²², and R²³ is selected independently from the group consisting of: methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, tert-butoxy, pentoxy, or neopentoxy. In some even further such embodiments, one of R²¹, R²², and R²³ is methoxy.

The siloxane polymers of any of the above embodiments can have any suitable physical properties. For example, in some embodiments, the siloxane polymer has a molecular weight ranging from 1 kDa to 50 kDa.

The siloxane polymers disclosed herein are made up primarily of constitutional units of formula (II) and constitutional units of formula (III). For example, in some embodiments, the constitutional units of formula (II) and the constitutional units of formula (III) together make up at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, of the constitutional units in the siloxane polymer.

The constitutional units of formula (II) can be present in any suitable quantity. For example, in some embodiments of any of the aforementioned embodiments, the constitutional units of formula (II) make up at least 10% by weight, or at least 20% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, of the constitutional units in the siloxane polymer. In some such embodiments, the constitutional units of formula (II) make up no more than 10% by weight, or no more than 20% by weight, or no more than 30% by weight, or no more than 40% by weight, or no more than 50% by weight, or no more than 60% by weight, or no more than 70% by weight, of the constitutional units in the siloxane polymer.

The constitutional units of formula (III) can be present in any suitable quantity. For example, in some embodiments of any of the aforementioned embodiments, the constitutional units of formula (III) make up at least 10% by weight, or at least 20% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, of the constitutional units in the siloxane polymer. In some such embodiments, the constitutional units of formula (III) make up no more than 10% by weight, or no more than 20% by weight, or no more than 30% by weight, or no more than 40% by weight, or no more than 50% by weight, or no more than 60% by weight, or no more than 70% by weight, of the constitutional units in the siloxane polymer.

The constitutional units of formula (II) can be present in any relative amount in comparison to the constitutional units of formula (III). For example, in some embodiments of any of the aforementioned embodiments, the numerical ratio of constitutional units of formula (I) to constitutional units of formula (III) in the siloxane polymer ranges from 1:5 to 5:1, or from 1:4 to 4:1, or from 1:3 to 3:1, or from 1:2 to 2:1.

The variables for each occurrence of a constitutional unit of formula (II) in the siloxane polymer can occur independently. For example, for each occurrence of a constitutional unit of formula (II), each R¹ can have different values, and each R² can have different values.

In some embodiments of any of the aforementioned embodiments, a minority of R¹ and R² are a hydrogen atom. For example, in some embodiments, of the constitutional units of formula (II) in the siloxane polymer, no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, of R¹ and R² are a hydrogen atom.

In some embodiments of any of the foregoing embodiments, at least half of R¹ and R² are a hydrocarbyl group. For example, in some embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, of R¹ and R² are C₁₋₁₄ hydrocarbyl. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, of R¹ and R² are C₁₋₆alkyl. In some even further embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl. In some even further embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, of R¹ and R² are substituents selected from the group consisting of methyl, ethyl, and isopropyl. And, in some even further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 50% by number, or at least 60% by number, or at least 70% by number, or at least 80% by number, or at least 90% by number, or at least 95% by number, of R¹ and R² are substituents are methyl.

The variables for each occurrence of a constitutional unit of formula (II) in the siloxane polymer can occur independently. For example, for each occurrence of a constitutional unit of formula (III), each R³ can have different values, and each R⁴ can have different values.

In some embodiments of any of the aforementioned embodiments, a minority of R³ and R⁴ are a hydrogen atom. For example, in some embodiments, of the constitutional units of formula (III) in the siloxane polymer, no more than 30% by number, or no more than 20% by number, or no more than 10% by number, or no more than 5% by number, of R³ and R⁴ are a hydrogen atom.

In some embodiments of any of the foregoing embodiments, some portion of R³ and R⁴ are a hydrocarbyl group. For example, in some such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 20% by number, or at least 30% by number, or at least 40% by number, or at least 50% by number, or at least 60% by number, or at least 70% by number, of R³ and R⁴ are C₁₋₁₄ hydrocarbyl. In some further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 20% by number, or at least 30% by number, or at least 40% by number, or at least 50% by number, or at least 60% by number, or at least 70% by number, of R³ and R⁴ are C₁₋₆alkyl. In some even further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 20% by number, or at least 30% by number, or at least 40% by number, or at least 50% by number, or at least 60% by number, or at least 70% by number, of R³ and R⁴ are substituents selected from the group consisting of methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and neopentyl. In some even further such embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 20% by number, or at least 30% by number, or at least 40% by number, or at least 50% by number, or at least 60% by number, or at least 70% by number, of R³ and R⁴ are substituents selected from the group consisting of methyl, ethyl, and isopropyl. In some even further such embodiments, of the constitutional units of formula (II) in the siloxane polymer, at least 20% by number, or at least 30% by number, or at least 40% by number, or at least 50% by number, or at least 60% by number, or at least 70% by number, of R³ and R⁴ are substituents are methyl.

The siloxane polymers disclosed herein include at least one constitutional unit of formula (III) where at least one of R³ and R⁴ is —(CH₂)_(n)C(═O)—R⁵. In general, in some number of constitutional units of formula (III), at least one of R³ and R⁴ is —(CH₂)_(n)C(═O)—R⁵. For example, in some embodiments of any of the aforementioned embodiments, of the constitutional units of formula (III) in the siloxane polymer, at least 10% by number, or at least 20% by number, or at least 30% by number, or at least 40% by number, or at least 50% by number, or at least 60% by number, or at least 70% by number, of R³ and R⁴ are —(CH₂)_(n)C(═O)—R⁵. Note that R⁵ is defined, independently for each occurrence within the siloxane polymer, according to any of the embodiments set forth above.

Methods of Making Siloxane Polymers

The siloxane polymers disclosed herein may be made in any suitable manner. For example, in some instances, a polysiloxane polymer can be made, where the polysiloxane polymer has Si—H side groups in the —Si—O—Si—O—Si—O— backbone. These groups can be reacted with functionalized terminally unsaturated fatty acids, such as functionalized derivatives of 9-decenoid acid, 10-undecenoic acid, and 11-dodecenoic acid, such that the carbon-carbon double bond reacts with the Si—H group to graft the functionalized fatty acid group onto the polysiloxane polymer.

Silicone Compositions

In one or more aspects, the present disclosure provides silicone compositions that comprise one or more siloxane polymers according to any of the embodiments set forth above. Such compositions can include the one or more siloxane polymers in any suitable concentration. For example, in some embodiments, the silicone polymer compositions comprise from 0.1 to 99 percent by weight, or from 0.5 to 99 percent by weight, or from 1 to 99 percent by weight, or from 5 to 99 percent by weight, of one or more siloxane polymers, based on the total weight of dry solids in the composition (i.e., the weight excluding the weight of any solvent(s), but including the weight of suspended or solvated non-solvent components).

In some embodiments, the silicone compositions disclosed herein include a carrier. Such compositions can include the one or more siloxane polymers in any suitable concentration. For example, in some embodiments, such silicone compositions comprise from 0.1 to 99 percent by weight, or from 0.5 to 99 percent by weight, or from 1 to 99 percent by weight, or from 5 to 99 percent by weight, based on the total weight of the composition. Any suitable carriers can be used. In some embodiments of any of the aforementioned embodiments, the carrier comprises water. In some other embodiments of any of the aforementioned embodiments, the carrier comprises an organic solvent.

The silicone compositions disclosed herein can also include one or more additives. For example, in some embodiments, the silicone composition includes one or more additives, such as surfactants, pigments, antimicrobial agents, photostabilizers, and the like.

The one or more siloxane polymers in the silicone compositions can have any suitable molecular weight range. For example, in some embodiments, the one or more siloxane polymers in the silicone composition have a weight-average molecular weight ranging from 1 kDa to 50 kDa.

Such silicone compositions can be used in any suitable way. For example, in some embodiments, the silicone composition is a surfactant composition, a sizing composition for a matrix reinforcement material (a silicaeous material, such as silica or sand; glass, such as glass fiber, glass particles, or glass beads; a metal, such as silver or titanium; a metal oxide, such as zinc oxide or titanium dioxide; carbon, such as carbon nanoparticles, carbon nanotubes, graphite, graphene, diamond, and fullerenes, or any combination of the foregoing), a coating composition, a sealant composition, a grease composition, a defoaming composition, a dry-cleaning composition, a rubber composition, an ophthalmic composition, a personal care composition, a lubricant composition, a personal lubricant composition, a functional fluid, such as a brake fluid, a mold release composition, a gel composition, or an electronics encasement composition.

Articles of Manufacture

In one or more aspects, the present disclosure provides articles of manufacture formed from the silicone compositions of any of the aforementioned embodiments. The article of manufacture can be any suitable article of manufacture, such as those that may typically be formed using silicone polymers. For example, in some embodiments, the article of manufacture is an electrical insulating article, an electronic device (where, for example, the silicone composition is in a coating or sealing layer), a gasket, a seal, a pad, a mold (such as, for example, a dental mold), a paper article (such as a sheet, where, for example, the silicone composition is in a coating), a textile article (where, for example, the silicone composition is in a coating), a fire stop, a microfluidic device, a bandage, a dressing for a wound, a scar treatment sheet, a breast implant, a testicular implant, a pectoral implant, a contact lens, an ophthalmic tube, an ophthalmic stent, or a nipple, such as a nipple on a baby bottle.

Derivation from Renewable Sources

The siloxane polymers disclosed herein and used in any of the aspects and embodiments disclosed herein can, in certain embodiments, be derived from renewable sources, such as various natural oils. Any suitable methods can be used to make these compounds from such renewable sources. Suitable methods include, but are not limited to, fermentation, conversion by bioorganisms, and conversion by metathesis.

Olefin metathesis provides one possible means to convert certain natural oil feedstocks into olefins and esters that can be used in a variety of applications, or that can be further modified chemically and used in a variety of applications. In some embodiments, a composition (or components of a composition) may be formed from a renewable feedstock, such as a renewable feedstock formed through metathesis reactions of natural oils and/or their fatty acid or fatty ester derivatives. When compounds containing a carbon-carbon double bond undergo metathesis reactions in the presence of a metathesis catalyst, some or all of the original carbon-carbon double bonds are broken, and new carbon-carbon double bonds are formed. The products of such metathesis reactions include carbon-carbon double bonds in different locations, which can provide unsaturated organic compounds having useful chemical properties.

A wide range of natural oils, or derivatives thereof, can be used in such metathesis reactions. Examples of suitable natural oils include, but are not limited to, vegetable oils, algae oils, fish oils, animal fats, tall oils, derivatives of these oils, combinations of any of these oils, and the like. Representative non-limiting examples of vegetable oils include rapeseed oil (canola oil), coconut oil, corn oil, cottonseed oil, olive oil, palm oil, peanut oil, safflower oil, sesame oil, soybean oil, sunflower oil, linseed oil, palm kernel oil, tung oil, jatropha oil, mustard seed oil, pennycress oil, camelina oil, hempseed oil, and castor oil. Representative non-limiting examples of animal fats include lard, tallow, poultry fat, yellow grease, and fish oil. Tall oils are by-products of wood pulp manufacture. In some embodiments, the natural oil or natural oil feedstock comprises one or more unsaturated glycerides (e.g., unsaturated triglycerides). In some such embodiments, the natural oil feedstock comprises at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, or at least 95% by weight, or at least 97% by weight, or at least 99% by weight of one or more unsaturated triglycerides, based on the total weight of the natural oil feedstock.

The natural oil may include canola or soybean oil, such as refined, bleached and deodorized soybean oil (i.e., RBD soybean oil). Soybean oil typically includes about 95 percent by weight (wt %) or greater (e.g., 99 wt % or greater) triglycerides of fatty acids. Major fatty acids in the polyol esters of soybean oil include but are not limited to saturated fatty acids such as palmitic acid (hexadecanoic acid) and stearic acid (octadecanoic acid), and unsaturated fatty acids such as oleic acid (9-octadecenoic acid), linoleic acid (9,12-octadecadienoic acid), and linolenic acid (9,12,15-octadecatrienoic acid).

Metathesized natural oils can also be used. Examples of metathesized natural oils include but are not limited to a metathesized vegetable oil, a metathesized algal oil, a metathesized animal fat, a metathesized tall oil, a metathesized derivatives of these oils, or mixtures thereof. For example, a metathesized vegetable oil may include metathesized canola oil, metathesized rapeseed oil, metathesized coconut oil, metathesized corn oil, metathesized cottonseed oil, metathesized olive oil, metathesized palm oil, metathesized peanut oil, metathesized safflower oil, metathesized sesame oil, metathesized soybean oil, metathesized sunflower oil, metathesized linseed oil, metathesized palm kernel oil, metathesized tung oil, metathesized jatropha oil, metathesized mustard oil, metathesized camelina oil, metathesized pennycress oil, metathesized castor oil, metathesized derivatives of these oils, or mixtures thereof. In another example, the metathesized natural oil may include a metathesized animal fat, such as metathesized lard, metathesized tallow, metathesized poultry fat, metathesized fish oil, metathesized derivatives of these oils, or mixtures thereof.

Such natural oils, or derivatives thereof, can contain esters, such as triglycerides, of various unsaturated fatty acids. The identity and concentration of such fatty acids varies depending on the oil source, and, in some cases, on the variety. In some embodiments, the natural oil comprises one or more esters of oleic acid, linoleic acid, linolenic acid, or any combination thereof. When such fatty acid esters are metathesized, new compounds are formed. For example, in embodiments where the metathesis uses certain short-chain olefins, e.g., ethylene, propylene, or 1-butene, and where the natural oil includes esters of oleic acid, an amount of 1-decene and 1-decenoid acid (or an ester thereof), among other products, are formed. Following transesterification, for example, with an alkyl alcohol, an amount of 9-denenoic acid alkyl ester is formed. In some such embodiments, a separation step may occur between the metathesis and the transesterification, where the alkenes are separated from the esters. In some other embodiments, transesterification can occur before metathesis, and the metathesis is performed on the transesterified product.

In some embodiments, the natural oil can be subjected to various pre-treatment processes, which can facilitate their utility for use in certain metathesis reactions. Useful pre-treatment methods are described in United States Patent Application Publication Nos. 2011/0113679, 2014/0275595, and 2014/0275681, all three of which are hereby incorporated by reference as though fully set forth herein.

In some embodiments, after any optional pre-treatment of the natural oil feedstock, the natural oil feedstock is reacted in the presence of a metathesis catalyst in a metathesis reactor. In some other embodiments, an unsaturated ester (e.g., an unsaturated glyceride, such as an unsaturated triglyceride) is reacted in the presence of a metathesis catalyst in a metathesis reactor. These polyol esters of unsaturated fatty acids may be a component of a natural oil feedstock, or may be derived from other sources, e.g., from esters generated in earlier-performed metathesis reactions. In certain embodiments, in the presence of a metathesis catalyst, the natural oil or unsaturated ester can undergo a self-metathesis reaction with itself. In other embodiments, the natural oil or unsaturated ester undergoes a cross-metathesis reaction with the low-molecular-weight olefin or mid-weight olefin. The self-metathesis and/or cross-metathesis reactions form a metathesized product wherein the metathesized product comprises olefins and esters.

In some embodiments, the low-molecular-weight olefin is in the C₂₋₆ range. As a non-limiting example, in one embodiment, the low-molecular-weight olefin may comprise at least one of: ethylene, propylene, 1-butene, 2-butene, isobutene, 1-pentene, 2-pentene, 3-pentene, 2-methyl-1-butene, 2-methyl-2-butene, 3-methyl-1-butene, cyclopentene, 1,4-pentadiene, 1-hexene, 2-hexene, 3-hexene, 4-hexene, 2-methyl-1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 2-methyl-2-pentene, 3-methyl-2-pentene, 4-methyl-2-pentene, 2-methyl-3-pentene, and cyclohexene. In some instances, a higher-molecular-weight olefin can also be used.

In some embodiments, the metathesis comprises reacting a natural oil feedstock (or another unsaturated ester) in the presence of a metathesis catalyst. In some such embodiments, the metathesis comprises reacting one or more unsaturated glycerides (e.g., unsaturated triglycerides) in the natural oil feedstock in the presence of a metathesis catalyst. In some embodiments, the unsaturated glyceride comprises one or more esters of oleic acid, linoleic acid, linoleic acid, or combinations thereof. In some other embodiments, the unsaturated glyceride is the product of the partial hydrogenation and/or the metathesis of another unsaturated glyceride (as described above). In some such embodiments, the metathesis is a cross-metathesis of any of the aforementioned unsaturated triglyceride species with another olefin, e.g., an alkene. In some such embodiments, the alkene used in the cross-metathesis is a lower alkene, such as ethylene, propylene, 1-butene, 2-butene, etc. In some embodiments, the alkene is ethylene. In some other embodiments, the alkene is propylene. In some further embodiments, the alkene is 1-butene. And in some even further embodiments, the alkene is 2-butene.

Metathesis reactions can provide a variety of useful products, when employed in the methods disclosed herein. For example, the polyol esters of unsaturated fatty acids may be derived from a natural oil feedstock, in addition to other valuable compositions. Moreover, in some embodiments, a number of valuable compositions can be targeted through the self-metathesis reaction of a natural oil feedstock, or the cross-metathesis reaction of the natural oil feedstock with a low-molecular-weight olefin or mid-weight olefin, in the presence of a metathesis catalyst. Such valuable compositions can include fuel compositions, detergents, surfactants, and other specialty chemicals. Additionally, transesterified products (i.e., the products formed from transesterifying an ester in the presence of an alcohol) may also be targeted, non-limiting examples of which include: fatty acid methyl esters (“FAMEs”); biodiesel; 9-decenoic acid (“9DA”) esters, 9-undecenoic acid (“9UDA”) esters, and/or 9-dodecenoic acid (“9DDA”) esters; 9DA, 9UDA, and/or 9DDA; alkali metal salts and alkaline earth metal salts of 9DA, 9UDA, and/or 9DDA; dimers of the transesterified products; and mixtures thereof.

Further, in some embodiments, multiple metathesis reactions can also be employed. In some embodiments, the multiple metathesis reactions occur sequentially in the same reactor. For example, a glyceride containing linoleic acid can be metathesized with a terminal lower alkene (e.g., ethylene, propylene, 1-butene, and the like) to form 1,4-decadiene, which can be metathesized a second time with a terminal lower alkene to form 1,4-pentadiene. In other embodiments, however, the multiple metathesis reactions are not sequential, such that at least one other step (e.g., transesterification, hydrogenation, etc.) can be performed between the first metathesis step and the following metathesis step. These multiple metathesis procedures can be used to obtain products that may not be readily obtainable from a single metathesis reaction using available starting materials. For example, in some embodiments, multiple metathesis can involve self-metathesis followed by cross-metathesis to obtain metathesis dimers, trimmers, and the like. In some other embodiments, multiple metathesis can be used to obtain olefin and/or ester components that have chain lengths that may not be achievable from a single metathesis reaction with a natural oil triglyceride and typical lower alkenes (e.g., ethylene, propylene, 1-butene, 2-butene, and the like). Such multiple metathesis can be useful in an industrial-scale reactor, where it may be easier to perform multiple metathesis than to modify the reactor to use a different alkene.

The conditions for such metathesis reactions, and the reactor design, and suitable catalysts are as described above with reference to the metathesis of the olefin esters. That discussion is incorporated by reference as though fully set forth herein.

In the embodiments above, the natural oil (e.g., as a glyceride) is metathesized, followed by transesterification. In some other embodiments, transesterification can precede metathesis, such that the fatty acid esters subjected to metathesis are fatty acid esters of monohydric alcohols, such as methanol, ethanol, or isopropanol.

Olefin Metathesis

In some embodiments, one or more of the unsaturated monomers can be made by metathesizing a natural oil or natural oil derivative. The terms “metathesis” or “metathesizing” can refer to a variety of different reactions, including, but not limited to, cross-metathesis, self-metathesis, ring-opening metathesis, ring-opening metathesis polymerizations (“ROMP”), ring-closing metathesis (“RCM”), and acyclic diene metathesis (“ADMET”). Any suitable metathesis reaction can be used, depending on the desired product or product mixture.

In some embodiments, after any optional pre-treatment of the natural oil feedstock, the natural oil feedstock is reacted in the presence of a metathesis catalyst in a metathesis reactor. In some other embodiments, an unsaturated ester (e.g., an unsaturated glyceride, such as an unsaturated triglyceride) is reacted in the presence of a metathesis catalyst in a metathesis reactor. These unsaturated esters may be a component of a natural oil feedstock, or may be derived from other sources, e.g., from esters generated in earlier-performed metathesis reactions. In certain embodiments, in the presence of a metathesis catalyst, the natural oil or unsaturated ester can undergo a self-metathesis reaction with itself. In other embodiments, the natural oil or unsaturated ester undergoes a cross-metathesis reaction with the low-molecular-weight olefin or mid-weight olefin. The self-metathesis and/or cross-metathesis reactions form a metathesized product wherein the metathesized product comprises olefins and esters.

In some embodiments, the low-molecular-weight olefin is in the C₂₋₆ range. As a non-limiting example, in one embodiment, the low-molecular-weight olefin may comprise at least one of: ethylene, propylene, 1-butene, 2-butene, isobutene, 1-pentene, 2-pentene, 3-pentene, 2-methyl-1-butene, 2-methyl-2-butene, 3-methyl-1-butene, cyclopentene, 1,4-pentadiene, 1-hexene, 2-hexene, 3-hexene, 4-hexene, 2-methyl-1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 2-methyl-2-pentene, 3-methyl-2-pentene, 4-methyl-2-pentene, 2-methyl-3-pentene, and cyclohexene. In some instances, a higher-molecular-weight olefin can also be used.

In some embodiments, the metathesis comprises reacting a natural oil feedstock (or another unsaturated ester) in the presence of a metathesis catalyst. In some such embodiments, the metathesis comprises reacting one or more unsaturated glycerides (e.g., unsaturated triglycerides) in the natural oil feedstock in the presence of a metathesis catalyst. In some embodiments, the unsaturated glyceride comprises one or more esters of oleic acid, linoleic acid, linoleic acid, or combinations thereof. In some other embodiments, the unsaturated glyceride is the product of the partial hydrogenation and/or the metathesis of another unsaturated glyceride (as described above). In some such embodiments, the metathesis is a cross-metathesis of any of the aforementioned unsaturated triglyceride species with another olefin, e.g., an alkene. In some such embodiments, the alkene used in the cross-metathesis is a lower alkene, such as ethylene, propylene, 1-butene, 2-butene, etc. In some embodiments, the alkene is ethylene. In some other embodiments, the alkene is propylene. In some further embodiments, the alkene is 1-butene. And in some even further embodiments, the alkene is 2-butene.

Metathesis reactions can provide a variety of useful products, when employed in the methods disclosed herein. For example, terminal olefins and internal olefins may be derived from a natural oil feedstock, in addition to other valuable compositions. Moreover, in some embodiments, a number of valuable compositions can be targeted through the self-metathesis reaction of a natural oil feedstock, or the cross-metathesis reaction of the natural oil feedstock with a low-molecular-weight olefin or mid-weight olefin, in the presence of a metathesis catalyst. Such valuable compositions can include fuel compositions, detergents, surfactants, and other specialty chemicals. Additionally, transesterified products (i.e., the products formed from transesterifying an ester in the presence of an alcohol) may also be targeted, non-limiting examples of which include: fatty acid methyl esters (“FAMEs”); biodiesel; 9-decenoic acid (“9DA”) esters, 9-undecenoic acid (“9UDA”) esters, and/or 9-dodecenoic acid (“9DDA”) esters; 9DA, 9UDA, and/or 9DDA; alkali metal salts and alkaline earth metal salts of 9DA, 9UDA, and/or 9DDA; dimers of the transesterified products; and mixtures thereof.

Further, in some embodiments, the methods disclosed herein can employ multiple metathesis reactions. In some embodiments, the multiple metathesis reactions occur sequentially in the same reactor. For example, a glyceride containing linoleic acid can be metathesized with a terminal lower alkene (e.g., ethylene, propylene, 1-butene, and the like) to form 1,4-decadiene, which can be metathesized a second time with a terminal lower alkene to form 1,4-pentadiene. In other embodiments, however, the multiple metathesis reactions are not sequential, such that at least one other step (e.g., transesterification, hydrogenation, etc.) can be performed between the first metathesis step and the following metathesis step. These multiple metathesis procedures can be used to obtain products that may not be readily obtainable from a single metathesis reaction using available starting materials. For example, in some embodiments, multiple metathesis can involve self-metathesis followed by cross-metathesis to obtain metathesis dimers, trimmers, and the like. In some other embodiments, multiple metathesis can be used to obtain olefin and/or ester components that have chain lengths that may not be achievable from a single metathesis reaction with a natural oil triglyceride and typical lower alkenes (e.g., ethylene, propylene, 1-butene, 2-butene, and the like). Such multiple metathesis can be useful in an industrial-scale reactor, where it may be easier to perform multiple metathesis than to modify the reactor to use a different alkene.

The metathesis process can be conducted under any conditions adequate to produce the desired metathesis products. For example, stoichiometry, atmosphere, solvent, temperature, and pressure can be selected by one skilled in the art to produce a desired product and to minimize undesirable byproducts. In some embodiments, the metathesis process may be conducted under an inert atmosphere. Similarly, in embodiments were a reagent is supplied as a gas, an inert gaseous diluent can be used in the gas stream. In such embodiments, the inert atmosphere or inert gaseous diluent typically is an inert gas, meaning that the gas does not interact with the metathesis catalyst to impede catalysis to a substantial degree. For example, non-limiting examples of inert gases include helium, neon, argon, and nitrogen, used individually or in with each other and other inert gases.

The rector design for the metathesis reaction can vary depending on a variety of factors, including, but not limited to, the scale of the reaction, the reaction conditions (heat, pressure, etc.), the identity of the catalyst, the identity of the materials being reacted in the reactor, and the nature of the feedstock being employed. Suitable reactors can be designed by those of skill in the art, depending on the relevant factors, and incorporated into a refining process such, such as those disclosed herein.

The metathesis reactions disclosed herein generally occur in the presence of one or more metathesis catalysts. Such methods can employ any suitable metathesis catalyst. The metathesis catalyst in this reaction may include any catalyst or catalyst system that catalyzes a metathesis reaction. Any known metathesis catalyst may be used, alone or in combination with one or more additional catalysts. Examples of metathesis catalysts and process conditions are described in US 2011/0160472, incorporated by reference herein in its entirety, except that in the event of any inconsistent disclosure or definition from the present specification, the disclosure or definition herein shall be deemed to prevail. A number of the metathesis catalysts described in US 2011/0160472 are presently available from Materia, Inc. (Pasadena, Calif.).

In some embodiments, the metathesis catalyst includes a Grubbs-type olefin metathesis catalyst and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes a first-generation Grubbs-type olefin metathesis catalyst and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes a second-generation Grubbs-type olefin metathesis catalyst and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes a first-generation Hoveyda-Grubbs-type olefin metathesis catalyst and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes a second-generation Hoveyda-Grubbs-type olefin metathesis catalyst and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes one or a plurality of the ruthenium carbene metathesis catalysts sold by Materia, Inc. of Pasadena, Calif. and/or one or more entities derived from such catalysts. Representative metathesis catalysts from Materia, Inc. for use in accordance with the present teachings include but are not limited to those sold under the following product numbers as well as combinations thereof: product no. C823 (CAS no. 172222-30-9), product no. C848 (CAS no. 246047-72-3), product no. C601 (CAS no. 203714-71-0), product no. C627 (CAS no. 301224-40-8), product no. C571 (CAS no. 927429-61-6), product no. C598 (CAS no. 802912-44-3), product no. C793 (CAS no. 927429-60-5), product no. C801 (CAS no. 194659-03-9), product no. C827 (CAS no. 253688-91-4), product no. C884 (CAS no. 900169-53-1), product no. C833 (CAS no. 1020085-61-3), product no. C859 (CAS no. 832146-68-6), product no. C711 (CAS no. 635679-24-2), product no. C933 (CAS no. 373640-75-6).

In some embodiments, the metathesis catalyst includes a molybdenum and/or tungsten carbene complex and/or an entity derived from such a complex. In some embodiments, the metathesis catalyst includes a Schrock-type olefin metathesis catalyst and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes a high-oxidation-state alkylidene complex of molybdenum and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes a high-oxidation-state alkylidene complex of tungsten and/or an entity derived therefrom. In some embodiments, the metathesis catalyst includes molybdenum (VI). In some embodiments, the metathesis catalyst includes tungsten (VI). In some embodiments, the metathesis catalyst includes a molybdenum- and/or a tungsten-containing alkylidene complex of a type described in one or more of (a) Angew. Chem. Int. Ed. Engl., 2003, 42, 4592-4633; (b) Chem. Rev., 2002, 102, 145-179; and/or (c) Chem. Rev., 2009, 109, 3211-3226, each of which is incorporated by reference herein in its entirety, except that in the event of any inconsistent disclosure or definition from the present specification, the disclosure or definition herein shall be deemed to prevail.

In certain embodiments, the metathesis catalyst is dissolved in a solvent prior to conducting the metathesis reaction. In certain such embodiments, the solvent chosen may be selected to be substantially inert with respect to the metathesis catalyst. For example, substantially inert solvents include, without limitation: aromatic hydrocarbons, such as benzene, toluene, xylenes, etc.; halogenated aromatic hydrocarbons, such as chlorobenzene and dichlorobenzene; aliphatic solvents, including pentane, hexane, heptane, cyclohexane, etc.; and chlorinated alkanes, such as dichloromethane, chloroform, dichloroethane, etc. In some embodiments, the solvent comprises toluene.

In other embodiments, the metathesis catalyst is not dissolved in a solvent prior to conducting the metathesis reaction. The catalyst, instead, for example, can be slurried with the natural oil or unsaturated ester, where the natural oil or unsaturated ester is in a liquid state. Under these conditions, it is possible to eliminate the solvent (e.g., toluene) from the process and eliminate downstream olefin losses when separating the solvent. In other embodiments, the metathesis catalyst may be added in solid state form (and not slurried) to the natural oil or unsaturated ester (e.g., as an auger feed).

The metathesis reaction temperature may, in some instances, be a rate-controlling variable where the temperature is selected to provide a desired product at an acceptable rate. In certain embodiments, the metathesis reaction temperature is greater than −40° C., or greater than −20° C., or greater than 0° C., or greater than 10° C. In certain embodiments, the metathesis reaction temperature is less than 200° C., or less than 150° C., or less than 120° C. In some embodiments, the metathesis reaction temperature is between 0° C. and 150° C., or is between 10° C. and 120° C.

The metathesis reaction can be run under any desired pressure. In some instances, it may be desirable to maintain a total pressure that is high enough to keep the cross-metathesis reagent in solution. Therefore, as the molecular weight of the cross-metathesis reagent increases, the lower pressure range typically decreases since the boiling point of the cross-metathesis reagent increases. The total pressure may be selected to be greater than 0.1 atm (10 kPa), or greater than 0.3 atm (30 kPa), or greater than 1 atm (100 kPa). In some embodiments, the reaction pressure is no more than about 70 atm (7000 kPa), or no more than about 30 atm (3000 kPa). In some embodiments, the pressure for the metathesis reaction ranges from about 1 atm (100 kPa) to about 30 atm (3000 kPa).

Examples

Preparation of the 9-Decenoic Acid Methyl Ester, 2a:

This material was obtained from Elevance Renewable Sciences (Woodridge, Ill.) and was used without any additional purification.

General Procedure for the Preparation of the Methyl Ester Ethoxylates, 2b & 2c:

Where:

-   -   2b has R=Triethylene glycol monomethyl ether ester     -   2c has R=Carbowax™ 750 MPEG

Into an appropriately sized 4-necked round-bottomed flask equipped with a heating mantle, magnetic stirrer, Dean-Stark trap, condenser, thermocouple with adaptor and J-Kem controller, glass stoppers, and a nitrogen inlet was added the alcohol followed by an equal molar amount of 9-decenoic acid (Elevance Renewable Sciences, Woodridge, Ill.). Toluene (0.25 vol %) (Sigma-Aldrich, St. Louis, Mo.) and acid catalyst (para-toluene sulfonic acid, pTsOH, 0.1 wt %) (Sigma-Aldrich, St. Louis, Mo.) were added and the reaction was stirred to homogenize. Heating was begun and the water collected in the Dean-Stark trap was periodically removed and measured to determine the reaction's progress. Occasionally, it was necessary to add an additional amounts of pTsOH to push the reaction to completion. Once the reaction was judged complete, the reaction was cooled to 100° C. and an equal weight of potassium carbonate (K₂CO₃) (Sigma-Aldrich, St. Louis, Mo.) to the pTsOH catalyst was added. This was stirred overnight at ambient temperature when a small sample was removed, dissolved into water, and its pH measured to ensure that the reaction mixture had been neutralized.

The reaction mixture was vacuum filtered through a pad of celite, and concentrated in vacuo to remove any residual toluene and reagents. The crude uC10MEE-03 (2b) material was vacuumed distilled at 142-148° C./0.3 torr to afford a clear, colorless liquid (97.2 area %) suitable for use in the hydrosilylation step. The uC10MEE-03 showed: FTIR (cm⁻¹) 2927 (m), 2857 (m), 1737 (s), 1640 (w), 1111 (vs), 911 (m); ¹H-NMR (ppm, CDCl₃) 5.8 (d of d of t, 1H), 4.9 (d of d, 2H), 4.2 (t, 2H), 3.6 (m, 8H), 3.5 (m, 2H), 3.4 (s, 3H), 2.3 (d of d, 2H), 2.0 (d of d, 2H), 1.6 (t, 2H), 1.3 (m, 8H)¹³C-NMR (ppm) 173.8, 139.0, 114.2, 71.9, 70.6, 70.5, 70.5, 69.2, 63.3, 59.0, 34.1, 33.7, 29.1, 29.0, 28.9, 28.8, 24.8; GC/MS (m/z) 316.2, 197.2, 99.0, 59.1. Alternatively, the tan-colored uC10MEE-16 solid could not be vacuum distilled overhead and was used without any additional purification. The high temperature gas chromatography analysis (HTGC) suggested that there was about 4% of unreacted MPEG left in the product.

Preparation of the 9-Decenoic-Nonafluoroester, uC10 Fluoro-Ester, 2d:

Into a 250 ml 3-necked round-bottomed flask equipped with a nitrogen inlet, stir bar, heating mantle, thermocouple with adaptor and J-Kem controller, condenser, and Dean-Stark trap was added in the 9-decenoic acid (9-DA, 24.6 g, 91% pure, 0.132 mol) (Elevance Renewable Sciences, Woodridge, Ill.), 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexanol (40.0 g, 0.152 mol, 1.15 equivalences), pTsOH (0.20 g, 1 mol %) and toluene (50 ml). The reaction was stirred, the nitrogen sweep begun, and heating applied to collect distillate in the pre-filled Dean-Stark trap. The reaction was monitored by the amount of water collected in the Dean-Stark trap and by FTIR as the reaction neared completion. Additional amounts of the fluoroalcohol can be added to drive the reaction to completion. The crude reaction product was washed with a saturated bicarbonate aqueous solution (1×25 ml), distilled water (2×25 ml) and dried through a cone of sodium sulfate.

The resulting organic phase was concentrated in vacuo and transferred into a 100 ml round-bottomed flask equipped with a short path distillation apparatus. Vacuum was applied and product was collected (83° C./0.44 torr) as a clear, colorless liquid (48.3 g, 97% pure, 85% yield). The uC10 fluoro ester showed: FTIR (cm⁻¹) 1745 (m), 1642 (w), 1234 (vs), 1221 (vs), 1167 (vs); 1H-NMR (ppm, CDCl₃) 5.8 (m, 1H), 4.9 (d of d, 2H), 4.4 (m, 2H), 2.4 (m, 2H), 2.3 (m, 2H), 2.0 (m, 2H), 1.6 (m, 2H), 1.3 (m, 8H); ¹³C-NMR (ppm) 173.3, 139.0, 114.1, 56.0, 34.0, 33.7, 30.6, 30.4, 30.2, 29.0, 29.0, 28.9, 28.8, 24.7; GC/MS (m/z) 416.2, 319, 152, 135, 110, 55.

General Grafting Procedure of the Derivatized Esters onto a Siloxane Oligomer:

Two commercial available, internally hydride-functionalized, siloxanes were reacted with the four previously prepared 9-decenoic acid derivatized esters (2a-d). The lower molecular weight, bis(trimethylsiloxy)methyl silane (3) was purchased from Sigma-Aldrich (St. Louis, Mo.), while the higher molecular weight Silmer™ H D2 (4) and H Di-10 (5) were obtained from SilTech Corporation (Lawrenceville, Ga.). Both the bis(trimethylsiloxy)methyl silane and the Silmer™ H D2 possessed internal hydride functionality, while the Silmer H Di-10 possessed terminal hydride functionality (shown in FIG. 3). All reactions were initiated by the addition of Karstedt's catalyst (Pt(0)-1,3-divinyl-1,1,3,3,-tetramethyl disiloxane complex solution) (Sigma-Aldrich, St. Louis, Mo.) at ambient temperatures.

(3) Bis(trimethylsiloxy)methyl silane: R═CH₃, R′═H, m=0, n=1 (MW=223)

(4) SilTech Silmer™ H D2: R═CH₃, R′═H (MW=1100, EqWt=270)

(5) SilTech Silmer™ H Di-10: R═H, R′═CH₃ (MW=875, EqWt=438)

The reactions were extremely exothermic and needed to be cooled by a dry ice bath once the temperature approached 30° C. For these reactions, an excess amount of terminal olefin substrate was used based on the equivalent weight (eqW) of hydrosiloxane. Reaction progress was monitored by FTIR as both the hydrosilane absorbance (2150 cm-1) and terminal olefin absorbance (1640 cm-1) disappeared while the carbonyl absorbance remained constant (1735 cm-1). Once the reaction was judged complete, the unreacted olefin starting material was removed by vacuum distillation. The resulting organofunctional siloxane oligomers were analyzed without further purification by 1H-NMR spectroscopy. Physical properties were determined and reported in Table 1 below.

Hydrosilylation Procedure:

Into either a 50 or 100 ml three-necked, round-bottomed flask equipped with a magnetic stirrer, a thermocouple with a J-Kem controller, a heating mantle and a short path distillation apparatus with a nitrogen inlet was added the uC10 derivative and the hydrosilane oligomer. In most cases the reaction was run neat, however the uC10MEE-16-based reactions were two phase so that isopropanol (IPOH) was added to compatiblize the reactants. Once the catalyst was added (1 drop) at ambient temperatures, the temperature was carefully monitored. The reaction was gentle warmed by an air gun until about 30° C. when heating was discontinued and a dry ice bath was used to moderate the vigorous exotherm. Once the temperature had stabilized, then the heating mantle was used to hold the reaction temperature at 60° C. for the next few hours. The reaction's progress was easily monitored by FTIR as both the hydrosilane absorbance (2150 cm⁻¹) and the terminal olefin's absorbance (1640 cm⁻¹) disappeared while the carbonyl absorbance remained constant (1735 cm⁻¹). When the reactions were judged complete, they were typically subjected to reduced pressure to remove any excess reagents or solvents. The products were transferred into 2 oz glass bottles and remained liquids except for the uC16MEE-16-based materials that solidified. A summary of the reactions is shown in Table 1 with Brookfield viscosities reported for each product.

TABLE 1 Grafted Siloxane Derivatives Amount of Amount of Equiv. of Surface Siloxane Ester Ester -per Yield Viscosity Tension Compound Reactants (g/mmol) (g/mmol) # of Si—H % (25° C.) (20° C.)  6 2a + 3 10.0 g 9.20 g 1.1 93 7.1 22.6 45.1 mmol 49.9 mmol  7 2b + 3 10.0 g 16.4 g 1.15 94 17 21.4 45.1 mmol 51.9 mmol  8 2c + 3 5.00 g 18.3 g 0.90 94 52 22.6 22.6 mmol 20.5 mmol  9 2d + 3 5.00 g 8.54 g 0.90 82 16 20.8 22.6 mmol 20.5 mmol 10 2a + 5 20.0 g 11.0 g 1.3 >99 17 18.9 22.9 mmol 59.8 mmol 11 2b + 5 20.0 g 21.7 g 1.5 >99 45 22.2 22.9 mmol 68.6 mmol 12 2c + 5 10.0 g 24.5 g 1.2 95 197 20.8 11.4 mmol 27.4 mmol 13 2d + 5 8.00 g 9.51 g 1.25 >99 34 21.3 9.1 mmol 22.8 mol 14 2a + 4 20.0 g 20.5 g 1.5 >99 71 22.0 18.2 mmol 111 mmol 15 2b + 4 15.0 g 26.4 g 1.5 >99 141 22.9 13.6 mmol 83.3 mmol 16 2c + 4 8.00 g 27.8 g 1.05 >99 232 21.2 7.3 mmol 31.1 mmol 17 2d + 4 6.00 g 10.2 g 1.1 >99 130 21.5 5.5 mmol 24.4 mmol Characterization of the grafted siloxane oligomers as follows:

Compound 6 (C₁₈H₄₂Si₃O₄): FTIR (cm⁻¹) 2926 (vw), 1745 (m), 1255 (m), 1045 (s), 840 (vs), 754 (m); ¹H-NMR (ppm, CDCl₃) 3.7 (s, 3H), 2.3 (t, 2H), 1.6 (m, 2H), 1.3 (br. m, 12H), 0.4 (t, 2H), 0.08 (s, 18H), −0.01 (s, 3H).

Compound 7 (C₂₄H₅₄Si₃O₇): FTIR (cm⁻¹) 2925 (vw), 1739 (m), 1254 (m), 1045 (s), 841 (vs), 755 (m); ¹H-NMR (ppm, CDCl₃) 4.2 (t, 2H), 3.7-3.5 (m, 10H), 3.4 (s, 3H), 2.3 (t, 2H), 1.6 (m, 2H), 1.3 (br. m, 12H), 0.4 (t, 2H), 0.7 (s, 18H), −0.02 (s, 3H).

Compound 8 (C₅₀H₁₀₆Si₃O₁₈): FTIR (cm⁻¹) 2886 (vw), 1737 (w), 1344 (m), 1111 (vs), 965 (m), 843 (s); 1H-NMR (ppm, CDCl₃) 4.3 (t, 2H), 3.8-3.5 (br. m, 62H), 3.4 (s, 3H), 2.3 (t, 2H), 1.6 (br, 10H), 1.3 (br., 14H), 0.4 (t, 2H), 0.8 (s, 13H), 0.01 (s, 20H).

Compound 9 (C₂₃H₄₃F₉Si₃O₄): FTIR (cm⁻¹) 2926 (vw), 1747 (m), 1235 (s), 1168 (s), 1048 (s), 841 (vs), 754 (m); 1H-NMR ppm, CDCl₃) 4.4 (t, 2H), 2.4 (m, 2H), 2.3 (t, 2H), 1.6 (m, 2H), 1.3 (br., 12H), 0.4 (t, 2H), 0.08 (s, 18H), −0.01 (s, 3H).

Compound 10 (C₄₆H₁₁₄Si₁₂O₁₅): FTIR (cm⁻¹) 2926 (vw), 1745 (m), 1259 (s), 1086 (s), 1020 (s), 797 (vs); 1H-NMR (ppm, CDCl₃) 5.8 (m, 0.2H uC10ME), 5.4 (m, 0.07H, isomerized uc10ME, 5.0 (m, 0.4H, uC10ME), 3.7 (s, 3H), 2.3 (t, 2H), 2.0 (m, 0.4H), 1.6 (t, 2H), 1.3 (br., 12H), 0.5 (t, 1.4H), 0.1-0.0 (m, 26H). Estimated to be 75% product and 25% uC10ME isomers.

Compound 11 (C₅₈H₁₃₈Si₁₂O₂₁): FTIR (cm⁻¹) 2924 (vw), 1739 (m) 1269 (s), 1089 (s) 1021 (s), 798 (vs); 1H-NMR (ppm, CDCl₃) 5.8 (m, 0.17H, uC10ME), 5.4 (m, 0.07H, isomerized uC10ME), 4.9 (m, 0.34H, uC10ME), 4.2 (t, 2H), 3.7-3.5 (m, 10H), 3.4 (s, 3H), 2.3 (t, 2H), 2.0 (m, 0.2H), 1.6 (m, 2H), 1.3 (br., 12H), 0.5 (t, 1.5H), 0.1-0.0 28H). Estimated to be 75% product and 25% uC10MEE-03 isomers.

Compound 12 (C₁₁₀H₂₄₂Si₁₂O₄₇): FTIR (cm⁻¹) 2883 (w), 1736 (w), 1260 (m), 1108 (vs), 1026 (s), 800 (vs); 1H-NMR (ppm, CDCl₃) 5.8 (m, 0.17H), 5.3 (m, 0.2H), 4.9 (m, 0.35H), 4.2 (t, 2H), 3.7-3.5 (m, 67H), 3.3 (s, 3H), 2.3 (t, 2H), 2.0 (m, 0.5H), 1.6 (m, 2H), 1.2 (br., 12H), (t, 1.3H), 0.20-0.0 (m, 30H)). Estimated to be 70% product and 30% uC10MEE-03 isomers.

Compound 13 (C₅₆H₁₁₆F₁₈Si₁₂O₁₅): FTIR (cm⁻¹) 2927 (vw), 1748 (w), 1259 (m), 1235 (m), 1086 (s), 1021 (s), 798 (vs); ¹H-NMR (ppm, CDCl₃) 5.8 (m, 0.2H, uC10 F-E), 5.4 (0.04H, isomerized uC10 F-E), 4.9 (m, 0.4H, uC10 F-E), 4.4 (t, 2H), 2.4 (m, 2H), 2.3 (t, 2H), 2.0 (m, 0.5H), 1.6 (m, 2H), 1.3 (m, 12H), 0.5 (t, 1.4H), 0.2-0.0, 27H). Estimated to be 75% product and 25% uC10 F-E isomers.

Compound 14 (C₇₃H₁₇₁Si_(15.5)O_(22.5)): FTIR (cm⁻¹) 2926 (vw), 1744 (m), 1259 (s), 1088 (s), 1018 (vs), 800 (vs); 1H-NMR (ppm, CDCl₃) 3.7 (s, 3H), 2.3 (t, 2H), 1.6 m, 2H), 1.3 (br., 12H), 0.5 (t, 2H), 1.0-0.0 (20H).

Compound 15 (C₉₇H₂₁₉Si_(15.5)O_(34.5)): FTIR (cm⁻¹) 2925 (w), 1738 (m), 1259 (s), 1092 (vs), 1019, (vs), 800 (vs); ¹H-NMR (ppm, CDCl₃) 5.8 (m, 0.4H, uC10MEE-03), 5.4 (m, 0.1H, isomerized uC10MEE-03), 4.9 (m, 0.09H, uC10MEE-03), 4.2 (t, 2H), 3.7-3.5 (m, 10H), 3.4 (s, 3H), 2.3 (t, 2H), 1.6 (d of d, 2H), 1.3 (br., 12H), 0.5 (t, 1.7H), 0.1-0.0 (m, 18H). Estimated to be 90% product and 10% uC10MEE-03 isomers.

Compound 16 (C₂₀₁H₄₂₇Si_(15.5)O_(86.5)): FTIR (cm⁻¹) 2865 (m), 1736 (w), 1259 (m), 1101 (vs), 1027 (s), 802 (s); 1H-NMR (ppm, CDCl₃) 5.5 (m, 0.26H), 4.4 (t, 2H), 2.3 (t, 2H), 1.6 (m, 2.7H0, 1.3 (br., 12H), 0.5 (m, 1.7H), 0.1-0.0 (m, 19H). Estimated to be 90% product.

Compound 17 (C₉₃H₁₇₅F₃₆Si_(15.5)O_(22.5)): FTIR (cm⁻¹) 2927 (vw), 1747 (w), 1259 (m), 1235 (m), 1088 (s), 1019 (vs), 801 (vs); ¹H-NMR (ppm, CDCl₃). 4 (m, 0.5H, isomerized uC10MEE-16), 4.2 (t, 1.7H), 3.7-3.5 (58H), 3.4 (s, 3H), 2.3 (t, 2H), 1.9 (m, 0.7H), 1.6 (m, 2H), 1.3 (br., 9H), 0.45 (m, 1H), 0.1-0.0, m, 17H). Estimated to be 75% product.

Hydrosiloxanes 3-5 are completely insoluble in water. Conversely, the three 2c grafted hybrid siloxanes (8, 12, 16) were considerably more water soluble (Table 2). This was determined by slowly adding these materials into stirred, ambient temperature, deionized water until the limit of solubility was reached (Table 2).

TABLE 2 Water Solubility of Siloxanes Grafted with 2c Grafting wt % Water Solubility Compound Sites of 2c (wt %)  8 Internal 79% 29% 12 Terminal 71% 31% 16 Internal 78% 26%

Hydrosiloxane 4 has very limited solubility in polar organic solvents. Conversely, compound 6 (i.e. 4 grafted with 2a) was significantly more soluble as shown in Table 3.

TABLE 3 Solubility in Organic Solvents Solubility (wt %) Ethyl- Com- Hep- Ace- Ace- Meth- ene pound tanes MEK tone tonitrile anol Glycol 4 >50 >50 >50  2  1 <1 6 >50 >50 >50 13 17  6 

What is claimed is:
 1. A siloxane polymer of formula (I):

wherein: each R¹, R², R³, and R⁴ is independently a hydrogen atom, a C₁₋₁₄ hydrocarbyl group, or a C₁₋₁₄ hydrocarbyloxy group; R^(x) and R^(y) are —(CH₂)_(n)C(═O)—R⁵—; each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹); each R⁶, R⁷, R⁸, and R⁹ is independently C₁₋₂₅ alkyl, C₂₋₂₅alkenyl, or C₁₋₁₀₁ heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R^(z); R^(z) is a halogen atom, —OH, —NH₂, C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₁₂ heteroalkyl, or C₆₋₁₄ aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; each n is independently an integer ranging from 9 to 17; and k is independently an integer ranging from 5 to
 5000. 2. The siloxane polymer of claim 1, wherein each R⁵ is independently —O—R⁶.
 3. The siloxane polymer of claim 2, wherein each R⁶ is independently C₁₋₁₂ alkyl.
 4. The siloxane polymer of claim 3, wherein each R⁶ is independently methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, or 2-ethylhexyl.
 5. The siloxane polymer of claim 2, wherein each R⁶ is independently C₃₋₄₀₁ oxyalkyl.
 6. The siloxane polymer of claim 5, wherein each R⁶ is independently —(CH₂—CH₂—O)_(w)—CH₃, wherein w is an integer ranging from 1 to
 200. 7. The siloxane polymer of claim 2, wherein each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more —OH groups, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group.
 8. The siloxane polymer of claim 2, wherein each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more halogen atoms.
 9. The siloxane polymer of claim 1, wherein each R⁵ is independently —NH—R⁷.
 10. The siloxane polymer of claim 9, wherein R⁷ is a moiety of formula (IV): -G³-N⁺—(R¹¹)(R¹²)-G⁴-R¹³  (IV) wherein: G³ is C₁₋₁₂ alkylene; G⁴ is C₁₋₆alkylene; R¹¹ and R¹² are independently a hydrogen atom or C₁₋₂₀ alkyl; and R¹³ is a hydrogen atom or a phenyl moiety.
 11. A siloxane polymer comprising a plurality of constitutional units, wherein the plurality of constitutional units comprises: (a) constitutional units of formula (II):

and (b) constitutional units of formula (III):

wherein: each R¹ and R² is independently a hydrogen atom, a C₃₋₁₀₁ oxyalkyl group, or a C₁₋₁₄ hydrocarbyl group, which is optionally substituted one or more times by halogen atoms; each R³ and R⁴ is independently a hydrogen atom, —(CH₂)_(n)C(═O)—R⁵, a C₃₋₁₀₁ oxyalkyl group, or a C₁₋₁₄ hydrocarbyl group, which is optionally substituted one or more times by halogen atoms, wherein, for each constitutional unit of formula (III), at least one of R³ and R⁴ is —(CH₂)_(n)C(═O)—R⁵; each R⁵ is independently —O—R⁶, —NH—R⁷, or —N(R⁸)(R⁹); each R⁶, R⁷, R⁸, and R⁹ is independently C₁₋₂₅ alkyl, C₂₋₂₅ alkenyl, or C₁₋₁₀₁ heteroalkyl, each of which is optionally substituted one or more times by substituents selected independently from R^(x); R^(x) is a halogen atom, —OH, —NH₂, C₁₋₆alkyl, C₂₋₆alkenyl, C₁₋₁₂ heteroalkyl, or C₆₋₁₄ aryl, wherein any two —OH substituents on immediately adjacent carbon atoms may optionally combine to form an epoxy group; and each n is independently an integer ranging from 9 to
 17. 12. The siloxane polymer of claim 11, wherein each R⁵ is independently —O—R⁶.
 13. The siloxane polymer of claim 12, wherein each R⁶ is independently C₁₋₁₂ alkyl.
 14. The siloxane polymer of claim 12, wherein each R⁶ is independently C₃₋₁₀₁ oxyalkyl.
 15. The siloxane polymer of claim 12, wherein each R⁶ is independently —(CH₂)_(x)—CH(O)CH₂, wherein x is an integer ranging from 1 to
 12. 16. The siloxane polymer of claim 12, wherein each R⁶ is independently C₁₋₁₂ alkyl, which is substituted by one or more halogen atoms.
 17. The siloxane polymer of claim 11, wherein each R⁵ is independently —NH—R⁷.
 18. The siloxane polymer of claim 17, wherein R⁷ is a moiety of formula (IV): -G³-N⁺—(R¹¹)(R¹²)-G⁴-R¹³  (IV) wherein: G³ is C₁₋₁₂ alkylene; G⁴ is C₁₋₆alkylene; R¹¹ and R¹² are independently a hydrogen atom or C₁₋₂₀ alkyl; and R¹³ is a hydrogen atom or a phenyl moiety.
 19. The siloxane polymer of claim 11, wherein the constitutional units of formula (II) and the constitutional units of formula (III) together make up at least 60% by weight of the constitutional units in the siloxane polymer.
 20. The siloxane polymer of claim 11, wherein the numerical ratio of constitutional units of formula (II) to constitutional units of formula (III) in the siloxane polymer ranges from 1:5 to 5:1, or from 1:4 to 4:1, or from 1:3 to 3:1, or from 1:2 to 2:1. 